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FDA 510(k)

PHYSIOLOGICAL PRESSURE TRANSDUCER

K-Number: K780477 · 1978-04-13

Decision Date1978-04-13
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Bell & Howell Instruments. It received FDA 510(k) clearance on 1978-04-13 under 510(k) number K780477. 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 PHYSIOLOGICAL PRESSURE TRANSDUCER?

PHYSIOLOGICAL PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1978-04-13. The listed applicant is Bell & Howell Instruments. The 510(k) number is K780477.

When did PHYSIOLOGICAL PRESSURE TRANSDUCER receive FDA 510(k) clearance?

PHYSIOLOGICAL PRESSURE TRANSDUCER received FDA 510(k) clearance on 1978-04-13, under 510(k) number K780477.

Who is the listed applicant for PHYSIOLOGICAL PRESSURE TRANSDUCER?

The FDA 510(k) record lists Bell & Howell Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHYSIOLOGICAL PRESSURE TRANSDUCER?

The FDA product code for PHYSIOLOGICAL PRESSURE TRANSDUCER is DRS.

Related Clinical Trials

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.

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.

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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