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

BIPOLATOR 50

K Number: K874779 · Decision Jan 29, 1988
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
80
Review Days
71

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Basic Information

Device Name
BIPOLATOR 50
K Number
K874779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Treace Medical, Inc.
Date Received
November 19, 1987
Decision Date
January 29, 1988
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 Treace Medical, Inc.

K Number Device Name
K883727 BUCKET PROSTHESIS PORP
K882349 MALLET, SURGICAL
K873154 TREACE MAGNUM OTO-TOOL SYSTEM
K872000 EYE GARD
K870765 CANNULATED INSTRUMENT CLEANERS
K871706 OPTHA PREP
K870759 CLEANING SOLUTION, CATALOG NO. 8203
K870766 PROSTHESIS WIRE
K870760 BUR BRUSH
K870763 SUPER SCISSORS
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