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

ST. MARK'S RECTAL BIOPSY FORCEPS

K Number: K822401 · Decision Aug 27, 1982
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
43
Applicant Total
29
Review Days
17

Basic Information

Device Name
ST. MARK'S RECTAL BIOPSY FORCEPS
K Number
K822401
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
KEYMED, INC.
Date Received
August 10, 1982
Decision Date
August 27, 1982
Product Code
KOA
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
KOA Surgical Instruments, G-U, Manual (And Accessories)

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