DIGI-PRO TENS MODEL WL-2203 AND WL-2205— 510(k) K021359

Substantially Equivalent

Well-Life Healthcare, Inc.

FDA 510(k) clearance K021359 for DIGI-PRO TENS MODEL WL-2203 AND WL-2205, Substantially Equivalent on 2002-04-30. Applicant: Well-Life Healthcare, Inc..

Clearance details

Applicant: Well-Life Healthcare, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 2002-01-30
Decision date: 2002-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung, R.O.C., TW

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