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

VALLEYLAB NS 2000 BIPOLAR GENERATOR SYSTEM

K Number: K946177 · Decision Jun 6, 1995
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
94
Review Days
169

Basic Information

Device Name
VALLEYLAB NS 2000 BIPOLAR GENERATOR SYSTEM
K Number
K946177
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
VALLEYLAB, INC.
Date Received
December 19, 1994
Decision Date
June 6, 1995
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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