FDA 510(k) K951104, ENDOBOOT, by United States Endoscopy Group, Inc.

510(K) Number: K951104
Device Name: ENDOBOOT
Manufacturer: United States Endoscopy Group, Inc.
Device Classification Name: endoscopic storage cover
Regulation Number: 876.1500
Classification Product Code: OCU
Date Received: 03/10/1995
Decision Date: 04/06/1995
Regulation Medical Specialty: Gastroenterology/Urology

Total pages: 36
Fully redacted pages: 4
Content pages: 32