TENS PRO 900— 510(k) K023726

Substantially Equivalent

Acumed Medical Supplies , Ltd.

FDA 510(k) clearance K023726 for TENS PRO 900, Substantially Equivalent on 2003-06-17. Applicant: Acumed Medical Supplies , Ltd.. Device class: 2.

Clearance details

Applicant: Acumed Medical Supplies , Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-11-06
Decision date: 2003-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.