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FDA 510(k)

ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN

K-Number: K811980 · 1981-07-28

ApplicantH.R. Biomedical, Ltd.
Decision Date1981-07-28
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN is the device name listed in this FDA 510(k) record. The listed applicant is H.R. Biomedical, Ltd.. It received FDA 510(k) clearance on 1981-07-28 under 510(k) number K811980. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN?

ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is H.R. Biomedical, Ltd.. The 510(k) number is K811980.

When did ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN receive FDA 510(k) clearance?

ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811980.

Who is the listed applicant for ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN?

The FDA 510(k) record lists H.R. Biomedical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN?

The FDA product code for ELECTRONIC BLOOD PRESSURE TRANSDUCER MAN is DRS.

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Related Devices (Code: DRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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