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

EZ STIM

K Number: K954505 · Decision Dec 10, 1996
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
28
Applicant Total
68
Review Days
439

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EZ STIM
K Number
K954505
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life-Tech Intl., Inc.
Date Received
September 28, 1995
Decision Date
December 10, 1996
Product Code
KOI
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
KOI Stimulator, Nerve, Peripheral, Electric

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KOI), ordered by most recent decision date.

View all

Other Clearances by Life-Tech Intl., Inc.

K Number Device Name
K001129 PROLONG, MODELS PL50, PL100, PL150
K955031 MAXISTIM
K954315 PVC ABDOMINAL/RECTAL PRESSURE CATHETER
K954341 URODYNAMICS TUBING AND INFUSION SETS
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. →