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

CLOSED-END/OPEN-END COLOSTOMY PCH. W/CON

K Number: K802677 · Decision Nov 12, 1980
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
101
Applicant Total
206
Review Days
14

Basic Information

Device Name
CLOSED-END/OPEN-END COLOSTOMY PCH. W/CON
K Number
K802677
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5900
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Johnson & Johnson Professionals, Inc.
Date Received
October 29, 1980
Decision Date
November 12, 1980
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

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