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FDA 510(k)

ELECTRONIC PERINEOMETER

K-Number: K800303 · 1980-03-03

ApplicantAssociates IN Biofeedback
Decision Date1980-03-03
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC PERINEOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Associates IN Biofeedback. It received FDA 510(k) clearance on 1980-03-03 under 510(k) number K800303. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC PERINEOMETER?

ELECTRONIC PERINEOMETER is a medical device that received FDA 510(k) clearance on 1980-03-03. The listed applicant is Associates IN Biofeedback. The 510(k) number is K800303.

When did ELECTRONIC PERINEOMETER receive FDA 510(k) clearance?

ELECTRONIC PERINEOMETER received FDA 510(k) clearance on 1980-03-03, under 510(k) number K800303.

Who is the listed applicant for ELECTRONIC PERINEOMETER?

The FDA 510(k) record lists Associates IN Biofeedback as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC PERINEOMETER?

The FDA product code for ELECTRONIC PERINEOMETER is HIR.

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Related Devices (Code: HIR)

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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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