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FDA 510(k)

MODEL MD-5 DOPPLER

K-Number: K901592 · 1990-10-22

ApplicantD. E. Hokanson, Inc.
Decision Date1990-10-22
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL MD-5 DOPPLER 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 1990-10-22 under 510(k) number K901592. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL MD-5 DOPPLER?

MODEL MD-5 DOPPLER is a medical device that received FDA 510(k) clearance on 1990-10-22. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K901592.

When did MODEL MD-5 DOPPLER receive FDA 510(k) clearance?

MODEL MD-5 DOPPLER received FDA 510(k) clearance on 1990-10-22, under 510(k) number K901592.

Who is the listed applicant for MODEL MD-5 DOPPLER?

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 MODEL MD-5 DOPPLER?

The FDA product code for MODEL MD-5 DOPPLER is DXK.

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Other records listing D. E. Hokanson, Inc. as applicant

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Related Devices (Code: DXK)

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

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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