§ 821.20. Devices subject to tracking.
94 words·~1 min read·
/us/cfr/t21/s§ 821.20·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(a)A manufacturer of any class II or class III device that fits within one of the three criteria within § 821.1(a) must track that device in accordance with this part, if FDA issues a tracking order to that manufacturer.
(b)When responding to premarket notification submissions and premarket approval applications, FDA will notify the sponsor by issuing an order that states that FDA believes the device meets the criteria of section 519(e)(1) of the act and, by virtue of the order, the sponsor must track the device. [67 FR 5951, Feb. 8, 2002]