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FDA 510(k)

CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER

K-Number: K023759 · 2003-05-06

ApplicantSonomedica
Decision Date2003-05-06
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Sonomedica. It received FDA 510(k) clearance on 2003-05-06 under 510(k) number K023759. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER?

CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER is a medical device that received FDA 510(k) clearance on 2003-05-06. The listed applicant is Sonomedica. The 510(k) number is K023759.

When did CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER receive FDA 510(k) clearance?

CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER received FDA 510(k) clearance on 2003-05-06, under 510(k) number K023759.

Who is the listed applicant for CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER?

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

What is the FDA product code for CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER?

The FDA product code for CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER is DQD.

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: DQD)

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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