BIOFEEDBACK DEVICE— 510(k) K954127

Substantially Equivalent

Verimed Holdings, Inc.

FDA 510(k) clearance K954127 for BIOFEEDBACK DEVICE, Substantially Equivalent on 1995-11-14. 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: 1995-08-31
Decision date: 1995-11-14
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.