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FDA 510(k)

THE PERCEPTOR(TM) STAND ALONE TRANSDUCER

K-Number: K910764 · 1991-04-22

Decision Date1991-04-22
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE PERCEPTOR(TM) STAND ALONE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1991-04-22 under 510(k) number K910764. 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 THE PERCEPTOR(TM) STAND ALONE TRANSDUCER?

THE PERCEPTOR(TM) STAND ALONE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1991-04-22. The listed applicant is North American Instrument Corp.. The 510(k) number is K910764.

When did THE PERCEPTOR(TM) STAND ALONE TRANSDUCER receive FDA 510(k) clearance?

THE PERCEPTOR(TM) STAND ALONE TRANSDUCER received FDA 510(k) clearance on 1991-04-22, under 510(k) number K910764.

Who is the listed applicant for THE PERCEPTOR(TM) STAND ALONE TRANSDUCER?

The FDA 510(k) record lists North American Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE PERCEPTOR(TM) STAND ALONE TRANSDUCER?

The FDA product code for THE PERCEPTOR(TM) STAND ALONE 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.

Other records listing North American Instrument Corp. as applicant

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.

View all 28 devices →

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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