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

MICROSURGICAL INSTRUMENTS

K Number: K874950 · Decision Dec 30, 1987
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
72
Applicant Total
13
Review Days
28

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Basic Information

Device Name
MICROSURGICAL INSTRUMENTS
K Number
K874950
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Solway, Inc.
Date Received
December 2, 1987
Decision Date
December 30, 1987
Product Code
HTD
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
HTD Forceps

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Other Clearances by Solway, Inc.

K Number Device Name
K874960 CARDIOVASCULAR SURGICAL INSTRUMENTS
K874962 FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS
K874956 SELF-RETAINING RETRACTOR FOR NEUROSURGERY
K874964 DENTAL HAND INSTRUMENTS
K875043 RONGEUR (NEUROSURGICAL INSTRUMENTS)
K874966 TUNING FORKS
K874959 VASCULAR CLAMP
K874954 MANUAL RONGEUR
K874952 MANUAL CRANIAL DRILL, BURR, TREPHINE & ACCESSORIES
K874965 MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE
Search all 13 clearances from Solway, Inc. →