21 C.F.R. · Food and Drugs
21 C.F.R. § 860.200

Purpose and applicability.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 860.200 — Purpose and applicability.

§ 860.200 Purpose and applicability. (a) The purpose of this part is to establish an efficient, transparent, and thorough process to facilitate De Novo classification into class I or class II for devices for which there is no legally marketed device on which to base a review of substantial equivalence and which meet the definition of class I or class II as described in section 513(a)(1) of the Federal Food, Drug, and Cosmetic Act and § 860.3. (b) De Novo requests can be submitted for a single device type: (1) After receiving a not substantially equivalent determination in response to a premarket notification (510(k)), or (2) If a person determines there is no legally marketed device upon which to base a determination of substantial equivalence.

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21 C.F.R. § 860.200
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The regulatory text of 21 C.F.R. § 860.200 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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