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

BIO-POLAR FORCEPS

K Number: K915826 · Decision Jun 2, 1992
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
14
Review Days
155

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Basic Information

Device Name
BIO-POLAR FORCEPS
K Number
K915826
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
Applied Medical
Date Received
December 30, 1991
Decision Date
June 2, 1992
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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K003443 SUCTION IRRIGATOR
K002915 FLEXIBLE OCCLUSION SYSTEM
K911462 SURGICAL TROCAR
K844673 APPLIED GAUZE SPONGE 4X4X16 PLY
K844677 APPLIED GAUZE SPONGE 2X2X12
K844674 APPLIED GAUZE SPONGE 2X2X8 PLY
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