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

EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS

K Number: K945975 · Decision Dec 21, 1994
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
21
Review Days
13

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Basic Information

Device Name
EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS
K Number
K945975
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
Everest Medical Corp.
Date Received
December 8, 1994
Decision Date
December 21, 1994
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 Everest Medical Corp.

K Number Device Name
K003060 PLASMAKINETIC GENERATOR
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K993412 BITX PROBES
K994336 BITX PROBES
K971565 BICOAG COAGULATING FORCEPS
K955001 EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS
K922509 LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA
K922246 TUBING SET W/ IRRIGATION & ASPIRATION VALVING
K920089 MONOPOLAR COAGULATING POLYPECTOMY SNARE
K911787 MONOPOLAR SPHINCTERTOME
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