BIOFEEDBACK MICROLAB— 510(k) K860271

Name: FDA 510(k) clearance K860271
Creator: U.S. Food and Drug Administration
Published: 1986-06-18

Substantially Equivalent

Hrm Software/Div. of Human Relations Media

FDA 510(k) clearance K860271 for BIOFEEDBACK MICROLAB, Substantially Equivalent on 1986-06-18. Applicant: Hrm Software/Div. of Human Relations Media. Device class: 2.

Clearance details

Applicant: Hrm Software/Div. of Human Relations Media
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1986-01-27
Decision date: 1986-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantville, 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.