MEGA-TENS DUAL CHANNEL T.E.N.S.— 510(k) K903017

Name: FDA 510(k) clearance K903017
Creator: U.S. Food and Drug Administration
Published: 1990-10-26

Substantially Equivalent

Futuremed Div. of Future Impex Corp.

FDA 510(k) clearance K903017 for MEGA-TENS DUAL CHANNEL T.E.N.S., Substantially Equivalent on 1990-10-26. Applicant: Futuremed Div. of Future Impex Corp.. Device class: 2.

Clearance details

Applicant: Futuremed Div. of Future Impex Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1990-07-10
Decision date: 1990-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerpark, NY, 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.