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FDA 510(k)

BIOFEEDBACK MICROLAB

K-Number: K860271 · 1986-06-18

ApplicantHrm Software/Div. of Human Relations Media
Decision Date1986-06-18
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BIOFEEDBACK MICROLAB is the device name listed in this FDA 510(k) record. The listed applicant is Hrm Software/Div. of Human Relations Media. It received FDA 510(k) clearance on 1986-06-18 under 510(k) number K860271. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOFEEDBACK MICROLAB?

BIOFEEDBACK MICROLAB is a medical device that received FDA 510(k) clearance on 1986-06-18. The listed applicant is Hrm Software/Div. of Human Relations Media. The 510(k) number is K860271.

When did BIOFEEDBACK MICROLAB receive FDA 510(k) clearance?

BIOFEEDBACK MICROLAB received FDA 510(k) clearance on 1986-06-18, under 510(k) number K860271.

Who is the listed applicant for BIOFEEDBACK MICROLAB?

The FDA 510(k) record lists Hrm Software/Div. of Human Relations Media as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOFEEDBACK MICROLAB?

The FDA product code for BIOFEEDBACK MICROLAB is HCC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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