THE DENVER SPLINT— 510(k) K791681

Substantially Equivalent

Xomed, Inc.

FDA 510(k) clearance K791681 for THE DENVER SPLINT, Substantially Equivalent on 1979-10-22. Applicant: Xomed, Inc..

Clearance details

Applicant: Xomed, Inc.
Product code: Code EPP
Advisory panel: Ear, Nose, Throat
Date received: 1979-08-28
Decision date: 1979-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arnold, MO, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.