TL250 INTERFERENTIAL/MUSCLE STIMULATOR INTERFERENTIAL CURRENT THERAPY MUSCLE STIMULATOR— 510(k) K990129

Name: FDA 510(k) clearance K990129
Creator: U.S. Food and Drug Administration
Published: 1999-04-12

Substantially Equivalent

Therapy Link, Inc.

FDA 510(k) clearance K990129 for TL250 INTERFERENTIAL/MUSCLE STIMULATOR INTERFERENTIAL CURRENT THERAPY MUSCLE STIMULATOR, Substantially Equivalent on 1999-04-12. Applicant: Therapy Link, Inc.. Device class: 2.

Clearance details

Applicant: Therapy Link, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1999-01-13
Decision date: 1999-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

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