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FDA 510(k)

BIOCOMP 2001 BIOFEEDBACK DEVICE

K-Number: K872495 · 1987-08-04

ApplicantBiofeedback Research Institute, Inc.
Decision Date1987-08-04
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BIOCOMP 2001 BIOFEEDBACK DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Biofeedback Research Institute, Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872495. 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 BIOCOMP 2001 BIOFEEDBACK DEVICE?

BIOCOMP 2001 BIOFEEDBACK DEVICE is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Biofeedback Research Institute, Inc.. The 510(k) number is K872495.

When did BIOCOMP 2001 BIOFEEDBACK DEVICE receive FDA 510(k) clearance?

BIOCOMP 2001 BIOFEEDBACK DEVICE received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872495.

Who is the listed applicant for BIOCOMP 2001 BIOFEEDBACK DEVICE?

The FDA 510(k) record lists Biofeedback Research Institute, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOCOMP 2001 BIOFEEDBACK DEVICE?

The FDA product code for BIOCOMP 2001 BIOFEEDBACK DEVICE 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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