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

PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE

K Number: K011787 · Decision Jul 6, 2001
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
11
Review Days
28

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Basic Information

Device Name
PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE
K Number
K011787
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vidamed, Inc.
Date Received
June 8, 2001
Decision Date
July 6, 2001
Product Code
KNS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNS Unit, Electrosurgical, Endoscopic (With Or Without 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
K002583 TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM
K973366 COBRA HAND PIECE
K965199 TUNA 5 CATHETER
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. →