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

BICOAG COAGULATING FORCEPS

K Number: K971565 · Decision Mar 12, 1998
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
15
Applicant Total
21
Review Days
317

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Basic Information

Device Name
BICOAG COAGULATING FORCEPS
K Number
K971565
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4150
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Everest Medical Corp.
Date Received
April 29, 1997
Decision Date
March 12, 1998
Product Code
HIN
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HIN Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HIN), ordered by most recent decision date.

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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
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. →