§814.108. Supplemental applications.
21 C.F.R. § 814.108
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.
Notes, amendments, and revision history
Amendments
[63 FR 59220, Nov. 3, 1998]
Source
Source: 61 FR 33244, June 26, 1996, unless otherwise noted.
Authority
Authority: 21 U.S.C. 351, 352, 353, 360, 360c-360j, 360bbb-8b, 371, 372, 373, 374, 375, 379, 379e, 379k-1, 381.
Source
Source: 51 FR 26364, July 22, 1986, unless otherwise noted.
Amendments
[63 FR 59220, Nov. 3, 1998]