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

BIOPLAR FORCEPS

K Number: K943231 · Decision Jul 26, 1994
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
104
Review Days
20

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Basic Information

Device Name
BIOPLAR FORCEPS
K Number
K943231
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
Cook Urological, Inc.
Date Received
July 6, 1994
Decision Date
July 26, 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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K082066 TAO BRUSH I.U.M.C. ENDOMETRIAL SAMPLER
K082536 COOK WIRE GUIDES
K082319 INJEKT FILIFORM INJECTION NEEDLE
K080525 COOK ODYSSEY HOLMIUM LASER SYSTEM, MODEL 30W
K073496 OPTILITE HOLMIUM LASER FIBERS
K072521 COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATH
K061371 SYDNEY IVF SPERM CRYOPRESERVATION BUFFER
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