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

STORZ S2050 SERIES BIPOLAR FORCEPS

K Number: K960009 · Decision Mar 6, 1996
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
101
Review Days
64

Basic Information

Device Name
STORZ S2050 SERIES BIPOLAR FORCEPS
K Number
K960009
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STORZ INSTRUMENT CO.
Date Received
January 2, 1996
Decision Date
March 6, 1996
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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