FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GRASPER, DISSECTOR, FORCEPS, NEEDLE HOLDER

K Number: K942574 · Decision Sep 28, 1994
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
78
Review Days
120

Basic Information

Device Name
GRASPER, DISSECTOR, FORCEPS, NEEDLE HOLDER
K Number
K942574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ACUFEX MICROSURGICAL, INC.
Date Received
May 31, 1994
Decision Date
September 28, 1994
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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