FDA 510(k), K833122, BURLINGTON ANTIMICROBIAL STOCKINEETTE

510(K) Number: K833122
Device Name: BURLINGTON ANTIMICROBIAL STOCKINEETTE
Manufacturer:
Device Classification Name: Drape, Surgical
Regulation Number: KKX
Classification Product Code: KXA
Date Received: 09/13/1983
Decision Date: 01/25/1984
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

27 pages (54 of 81 original pages are fully redacted)