MYOEXORCISER II FUAL— 510(k) K951969

Substantially Equivalent

Verimed Holdings, Inc.

FDA 510(k) clearance K951969 for MYOEXORCISER II FUAL, Substantially Equivalent on 1995-06-14. Applicant: Verimed Holdings, Inc.. Device class: 2.

Clearance details

Applicant: Verimed Holdings, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1995-04-27
Decision date: 1995-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Coral Springs, FL, 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.