21 CFR § 814.108 Premarket Approval of Medical Devices

§ 814.108 Supplemental applications.

Current through Sep 8, 2026 · Read all of Part 814

After FDA approval of an original HDE, an applicant shall submit supplements in accordance with the requirements for PMA's under § 814.39, except that a request for a new indication for use of a HUD shall comply with requirements set forth in § 814.110. The timeframes for review of, and FDA action on, an HDE supplement are the same as those provided in § 814.114 for an HDE.

[63 FR 59220, Nov. 3, 1998]

← § 814.106 HDE amendments and resubmitted HDE's.§ 814.110 New indications for use. →