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

ELECTROSURGICAL CUTTING & COAGULATION DEVICE ACCESSORIES

K Number: K945254 · Decision Jun 6, 1995
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
221

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Basic Information

Device Name
ELECTROSURGICAL CUTTING & COAGULATION DEVICE ACCESSORIES
K Number
K945254
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
Endotec, Inc.
Date Received
October 28, 1994
Decision Date
June 6, 1995
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 Endotec, Inc.

K Number Device Name
K081400 FANNING-PAPPAS MODULAR KNEE BEARING
K012702 BUECHEL-PAPPAS (B-P) FIXED BEARING NEW JERSEY (NJ) TOTAL KNEE, MODEL 1
K992394 BUECHEL-PAPPAS HUMERAL HEAD RESURFACING COMPONENT
K982418 BUECHEL-PAPPAS MODULAR SALVAGE STEM
K963101 B-P HEMISPHERICAL ACETABULAR COMPONENT
K963100 TRONZO ACETABULAR FIXATION COMPONENT (1 99-02-00XX (ACE. FIXATION CUP) XX=OD OF ACE. CUP
K960425 BUECHEL-PAPPAS POLYETHLENE ACETABULAR COMPONENT(01-42-YYXX & 01-43-YYXX
K960424 BUECHEL-PAPPAS POLYETHYLENE GLENOID COMPONENT (02-11-YYXX) NOTE:YY=ID & XX=OD
K944465 CARRIER, LIGATURE (79 GEJ)
K944414 DEKALB
Search all 15 clearances from Endotec, Inc. →