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FDA 510(k)

P-1 ULTRASONIC ARTERIOGRAPH

K-Number: K761288 · 1976-12-28

ApplicantD. Eugene Hokanson
Decision Date1976-12-28
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

P-1 ULTRASONIC ARTERIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is D. Eugene Hokanson. It received FDA 510(k) clearance on 1976-12-28 under 510(k) number K761288. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-1 ULTRASONIC ARTERIOGRAPH?

P-1 ULTRASONIC ARTERIOGRAPH is a medical device that received FDA 510(k) clearance on 1976-12-28. The listed applicant is D. Eugene Hokanson. The 510(k) number is K761288.

When did P-1 ULTRASONIC ARTERIOGRAPH receive FDA 510(k) clearance?

P-1 ULTRASONIC ARTERIOGRAPH received FDA 510(k) clearance on 1976-12-28, under 510(k) number K761288.

Who is the listed applicant for P-1 ULTRASONIC ARTERIOGRAPH?

The FDA 510(k) record lists D. Eugene Hokanson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P-1 ULTRASONIC ARTERIOGRAPH?

The FDA product code for P-1 ULTRASONIC ARTERIOGRAPH is DPW.

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Related Devices (Code: DPW)

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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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