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

URODYNAMICS TUBING AND INFUSION SETS

K Number: K954341 · Decision Oct 17, 1995
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
35
Applicant Total
68
Review Days
29

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Basic Information

Device Name
URODYNAMICS TUBING AND INFUSION SETS
K Number
K954341
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1620
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life-Tech Intl., Inc.
Date Received
September 18, 1995
Decision Date
October 17, 1995
Product Code
FEN
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
FEN Device, Cystometric, Hydraulic

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Other Clearances by Life-Tech Intl., Inc.

K Number Device Name
K001129 PROLONG, MODELS PL50, PL100, PL150
K955031 MAXISTIM
K954505 EZ STIM
K954315 PVC ABDOMINAL/RECTAL PRESSURE CATHETER
K953451 UROPUMP TUBE & DAMPING CHAMGER
K953353 UROVISION JANUS
K946108 EAR-A-GATOR
K913601 MICROPHOR
K940203 TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS
K931179 UROLAB SPECTRUM
Search all 68 clearances from Life-Tech Intl., Inc. →