INTERCEPT T.E.N.S. DEVICE— 510(k) K880492

Name: FDA 510(k) clearance K880492
Creator: U.S. Food and Drug Administration
Published: 1988-04-18

Substantially Equivalent

Medical Design & Manufacturing Corp.

FDA 510(k) clearance K880492 for INTERCEPT T.E.N.S. DEVICE, Substantially Equivalent on 1988-04-18. Applicant: Medical Design & Manufacturing Corp.. Device class: 2.

Clearance details

Applicant: Medical Design & Manufacturing Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-02-04
Decision date: 1988-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westerville, OH, US

Download summary PDF View on FDA.gov ↗

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