Fabio
76b8ec33a7
Ingested titles 12–51 and 54 from OLRC USLM XML @119-100 (the whole Code now, uniform edition; Title 53 is reserved/empty). LegalText 11,221 -> 59,740; repo total 105,704 records. Deterministic (byte-identical rerun, verified on Title 42's 8,356 sections); make check green. make legal-us-code default now covers every title. Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
48 lines
1.8 KiB
Markdown
48 lines
1.8 KiB
Markdown
---
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type: "LegalText"
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title: "21 U.S.C. § 360c–1"
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description: "Reporting"
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jurisdiction: "us"
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corpus: "united_states_code"
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kind: "code_section"
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title_number: 21
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title_name: "FOOD AND DRUGS"
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chapter_number: "9"
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chapter_name: "FEDERAL FOOD, DRUG, AND COSMETIC ACT"
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section: "360c–1"
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citation: "21 U.S.C. § 360c–1"
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status: "current"
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release_point: "119-100"
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release_date: "2026-06-26"
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source: "official"
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source_url: "https://uscode.house.gov/download/releasepoints/us/pl/119/100/xml_usc21@119-100.zip"
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source_identifier: "/us/usc/t21/s360c–1"
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source_file: "data/legal/raw/us/code/title-21/usc21.xml"
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source_hash: "8b9ffc87defb6ff20f0374330fd536a09743329c55141e715193079cab1f782c"
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raw_snapshot_hash: "3dbd7a61c8616baefb8459bd8dac3b93242106deb416308c8d4dd5a9143176d1"
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text_hash: "836bdfdbeb52a36045aa103b0beea3779d9c23e36e8cf2bef6f545489bf9578a"
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retrieved_at: "2026-07-04"
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confidence: "official"
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tags: ["legal", "us-code"]
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---
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# 21 U.S.C. § 360c–1 - Reporting
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## Text
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The Secretary of Health and Human Services shall annually post on the Internet Web site of the Food and Drug Administration—
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(1) the number and type of class I and class II devices reclassified as class II or class III in the previous calendar year under section 360c(e)(1) of this title;
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(2) the number and type of class II and class III devices reclassified as class I or class II in the previous calendar year under such section 360c(e)(1) of this title; and
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(3) the number and type of devices reclassified in the previous calendar year under section 360e of this title.
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(Pub. L. 112–144, title VI, § 608(c), July 9, 2012, 126 Stat. 1059.)
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## Notes
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Editorial Notes
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Codification Section was enacted as part of the Food and Drug Administration Safety and Innovation Act, and not as part of the Federal Food, Drug, and Cosmetic Act which comprises this chapter.
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