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

PLASTIC THUMB FORCEPS

K Number: K831664 · Decision Sep 12, 1983
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
20
Review Days
112

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Basic Information

Device Name
PLASTIC THUMB FORCEPS
K Number
K831664
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
May 23, 1983
Decision Date
September 12, 1983
Product Code
KDC
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
KDC Instrument, Surgical, Disposable

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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
K831665 DISPOSABLE NEEDLE HOLDER
K831661 DISPOSABLE SCISSORS
K831662 DISPOSABLE HEMOSTAT (STRAIGHT&CURVED
K823854 MEDCARE SUTURE REMOVAL TRAYS
K823853 MEDCARE WOUND CLOSURE TRAY
Search all 20 clearances from Medcare Products →