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

BITX PROBES

K Number: K994336 · Decision Feb 8, 2000
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
21
Review Days
47

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Basic Information

Device Name
BITX PROBES
K Number
K994336
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 23, 1999
Decision Date
February 8, 2000
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
K000496 EVERSHEARS BIPOLAR SCISSORS
K993412 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
K911787 MONOPOLAR SPHINCTERTOME
Search all 21 clearances from Everest Medical Corp. →