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

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS

K Number: K874962 · Decision Feb 2, 1988
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
33
Applicant Total
13
Review Days
62

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Basic Information

Device Name
FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS
K Number
K874962
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.4535
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Solway, Inc.
Date Received
December 2, 1987
Decision Date
February 2, 1988
Product Code
HAO
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HAO Instrument, Surgical, Non-Powered

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Other Clearances by Solway, Inc.

K Number Device Name
K874960 CARDIOVASCULAR SURGICAL INSTRUMENTS
K874956 SELF-RETAINING RETRACTOR FOR NEUROSURGERY
K874964 DENTAL HAND INSTRUMENTS
K875043 RONGEUR (NEUROSURGICAL INSTRUMENTS)
K874966 TUNING FORKS
K874950 MICROSURGICAL INSTRUMENTS
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. →