TENS DEVICE FOR RELIEF OF CHRONIC PAIN— 510(k) K864114

Name: FDA 510(k) clearance K864114
Creator: U.S. Food and Drug Administration
Published: 1987-04-01

Substantially Equivalent

Futuremed Div. of Future Impex Corp.

FDA 510(k) clearance K864114 for TENS DEVICE FOR RELIEF OF CHRONIC PAIN, Substantially Equivalent on 1987-04-01. 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: 1986-10-21
Decision date: 1987-04-01
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.