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

MODEL 20 BIPOLAR COAGULATOR

K Number: K972311 · Decision Sep 18, 1997
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
17
Review Days
90

Basic Information

Device Name
MODEL 20 BIPOLAR COAGULATOR
K Number
K972311
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
BOSTON SURGICAL PRODUCTS, INC.
Date Received
June 20, 1997
Decision Date
September 18, 1997
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 BOSTON SURGICAL PRODUCTS, INC.

K Number Device Name
K972350 MODEL 50 BIPOLAR COAGULATOR
K944947 ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESS
K953012 DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLS
K950375 DISPOSABLE & REUSABLE BIPOLAR SUCTION COAGULATOR
K951912 DISOPOSABLE & RESUABLE MONPOLAR CORD
K951269 DISPOSABLE & REUSABLE MONOPOLAR HANDSWITHC PENCIL
K950877 REUSABLE MONOPOLAR FORCEPS
K945171 DISPOSABLE & RESUABLE IRRIGATION/ASPIRATION HANDPIECE
K945893 DISPOSABLE & REUSABLE MONOPOLAR ELECTROSURIGICAL ELECTRODE
K944642 ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES
Search all 17 clearances from BOSTON SURGICAL PRODUCTS, INC. →