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

TUNA 5 CATHETER

K Number: K965199 · Decision Apr 30, 1997
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
125

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Basic Information

Device Name
TUNA 5 CATHETER
K Number
K965199
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
Vidamed, Inc.
Date Received
December 26, 1996
Decision Date
April 30, 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 Vidamed, Inc.

K Number Device Name
K014224 PRECISION PLUS TUNA OFFICE SYSTEM
K012587 RF GENERATORS, DISPOSABLE CARTRIDGE KIT, DISPOSABLE CARTRIDGE, REUSABLE HANDLE, DISOISABLE HANDPIECE REUSABLE TELESCOPE
K011787 PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE
K002583 TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM
K973366 COBRA HAND PIECE
K965061 VIDAMED MODEDL 7600 RF GENERATOR
K963180 VIDAMED RF GENERATOR DATA RECORDER
K960918 VIDAMED TUNA (TRANSURETHRAL NEEDLE ABLATION) SYSTEM
K955035 VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR
K951245 VIDAMED 50 ELECTROSURGICAL GENERATOR, VIDAMED AEC (ADJUSTABLE ELECTROSURGICAL CARTRIDGE) ACCESSORY
Search all 11 clearances from Vidamed, Inc. →