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

LAMINATED KARAYA GUM WASHERS

K Number: K820167 · Decision Feb 18, 1982
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
101
Applicant Total
3
Review Days
28

Basic Information

Device Name
LAMINATED KARAYA GUM WASHERS
K Number
K820167
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5900
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Atlantic Surgical
Date Received
January 21, 1982
Decision Date
February 18, 1982
Product Code
EXB
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
EXB Collector, Ostomy

Similar 510(k) Clearances

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

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Other Clearances by Atlantic Surgical

K Number Device Name
K772366 BAG, DRAINAGEW/ADHESIVE; PROSTHESIS
K770230 KARAYA GUM POWDER