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

TRACER

K Number: K881842 · Decision Aug 31, 1988
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
68
Review Days
121

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Basic Information

Device Name
TRACER
K Number
K881842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Life-Tech Intl., Inc.
Date Received
May 2, 1988
Decision Date
August 31, 1988
Product Code
BXN
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
BXN Stimulator, Nerve, Battery-Powered

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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
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
Search all 68 clearances from Life-Tech Intl., Inc. →