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

GM MONOPOLAR/FRAZIER SUCTION PROBE

K Number: K934035 · Decision Dec 1, 1993
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
105

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Basic Information

Device Name
GM MONOPOLAR/FRAZIER SUCTION PROBE
K Number
K934035
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gm Engineering, Inc.
Date Received
August 18, 1993
Decision Date
December 1, 1993
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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Other Clearances by Gm Engineering, Inc.

K Number Device Name
K953348 ARTICULATING RETRACTOR TISSUE RETRACTORS
K942626 CONTINUOUS FLOW BIOPSY PROBE
K932394 BERNSTEIN(TM) UTERINE MANIPULATOR
K941661 GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT
K942703 GM REUSABLE AND DISPOSABLE TROCAR AND GM REUSABLE AND DISPOSABLE ULTRA-LIGHT CANNULA
K941662 GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHT
K941660 GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT
K933962 GM CONTINUOUS FLOW BIOPSY PROBE
K930611 TRUE FLOW(TM) VALVE
K931398 GM SWIVEL VIDEO (TM) IRRIGATOR
Search all 11 clearances from Gm Engineering, Inc. →