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

TISSUE FORCEPS

K Number: K822591 · Decision Oct 13, 1982
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
20
Review Days
35

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Basic Information

Device Name
TISSUE FORCEPS
K Number
K822591
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Medcare Products
Date Received
September 8, 1982
Decision Date
October 13, 1982
Product Code
GEN
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEN Forceps, General & Plastic Surgery

Similar 510(k) Clearances

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

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Other Clearances by Medcare Products

K Number Device Name
K841122 TRACHEOSTOMY CARE TRAY
K841124 DIALYSIS TRAY
K841123 DRESSING CHANGE TRAY
K831374 MED CARE PREP RAZOR
K831663 TISSUE FORCEPS
K831664 PLASTIC THUMB FORCEPS
K831665 DISPOSABLE NEEDLE HOLDER
K831661 DISPOSABLE SCISSORS
K831662 DISPOSABLE HEMOSTAT (STRAIGHT&CURVED
K823854 MEDCARE SUTURE REMOVAL TRAYS
Search all 20 clearances from Medcare Products →