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FDA 510(k)

P-2 ULTRASONIC ARTERIOGRAPH

K-Number: K792015 · 1979-12-04

ApplicantD. E. Hokanson, Inc.
Decision Date1979-12-04
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

P-2 ULTRASONIC ARTERIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is D. E. Hokanson, Inc.. It received FDA 510(k) clearance on 1979-12-04 under 510(k) number K792015. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-2 ULTRASONIC ARTERIOGRAPH?

P-2 ULTRASONIC ARTERIOGRAPH is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K792015.

When did P-2 ULTRASONIC ARTERIOGRAPH receive FDA 510(k) clearance?

P-2 ULTRASONIC ARTERIOGRAPH received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792015.

Who is the listed applicant for P-2 ULTRASONIC ARTERIOGRAPH?

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

What is the FDA product code for P-2 ULTRASONIC ARTERIOGRAPH?

The FDA product code for P-2 ULTRASONIC ARTERIOGRAPH is DPT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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