TTECH MODEL 200E + TENS DEVICE— 510(k) K021436

Substantially Equivalent

Theratech, Inc.

FDA 510(k) clearance K021436 for TTECH MODEL 200E + TENS DEVICE, Substantially Equivalent on 2002-07-30. Applicant: Theratech, Inc.. Device class: 2.

Clearance details

Applicant: Theratech, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-05-06
Decision date: 2002-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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