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

LAPAROSCOPIC ELECTROSURGICAL DEVICE

K Number: K904993 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
21
Review Days
79

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Basic Information

Device Name
LAPAROSCOPIC ELECTROSURGICAL DEVICE
K Number
K904993
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Everest Medical Corp.
Date Received
November 7, 1990
Decision Date
January 25, 1991
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

Similar 510(k) Clearances

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Other Clearances by Everest Medical Corp.

K Number Device Name
K003060 PLASMAKINETIC GENERATOR
K000496 EVERSHEARS BIPOLAR SCISSORS
K993412 BITX PROBES
K994336 BITX PROBES
K971565 BICOAG COAGULATING FORCEPS
K955001 EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS
K945975 EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS
K922509 LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA
K922246 TUBING SET W/ IRRIGATION & ASPIRATION VALVING
K920089 MONOPOLAR COAGULATING POLYPECTOMY SNARE
Search all 21 clearances from Everest Medical Corp. →