CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898) > PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES > SUBPART H—Humanitarian Use Devices (§814.100 to §814.126) > 814.108—Supplemental applications.

814.108—Supplemental applications.

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.

Code of Federal Regulations

[63 FR 59220, Nov. 3, 1998]