VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE &— 510(k) K853992

Name: FDA 510(k) clearance K853992
Creator: U.S. Food and Drug Administration
Published: 1986-02-21

Substantially Equivalent

Valley Forge Scientific Corp.

FDA 510(k) clearance K853992 for VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE &, Substantially Equivalent on 1986-02-21. Applicant: Valley Forge Scientific Corp.. Device class: 2.

Clearance details

Applicant: Valley Forge Scientific Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1985-09-27
Decision date: 1986-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valley Forge, PA, US

Download summary PDF View on FDA.gov ↗

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