FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BAG, DRAINAGEW/ADHESIVE; PROSTHESIS

K Number: K772366 · Decision Jan 26, 1978
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
2
Applicant Total
3
Review Days
30

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BAG, DRAINAGEW/ADHESIVE; PROSTHESIS
K Number
K772366
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5900
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Atlantic Surgical
Date Received
December 27, 1977
Decision Date
January 26, 1978
Product Code
FON
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FON Bag, Drainage, With Adhesive, Ostomy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FON), ordered by most recent decision date.

View all

Other Clearances by Atlantic Surgical

K Number Device Name
K820167 LAMINATED KARAYA GUM WASHERS
K770230 KARAYA GUM POWDER