THE FM-212A BIOFEEDBACK UNIT— 510(k) K861950

Name: FDA 510(k) clearance K861950
Creator: U.S. Food and Drug Administration
Published: 1987-04-22

Substantially Equivalent

Hosa Technology, Inc.

FDA 510(k) clearance K861950 for THE FM-212A BIOFEEDBACK UNIT, Substantially Equivalent on 1987-04-22. Applicant: Hosa Technology, Inc.. Device class: 2.

Clearance details

Applicant: Hosa Technology, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1986-05-20
Decision date: 1987-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cerritos, CA, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.