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FDA 510(k)

DCG-VII ELECTROCARDIOSCANNER

K-Number: K791424 · 1979-08-28

Decision Date1979-08-28
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DCG-VII ELECTROCARDIOSCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Del Mar Avionics. It received FDA 510(k) clearance on 1979-08-28 under 510(k) number K791424. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DCG-VII ELECTROCARDIOSCANNER?

DCG-VII ELECTROCARDIOSCANNER is a medical device that received FDA 510(k) clearance on 1979-08-28. The listed applicant is Del Mar Avionics. The 510(k) number is K791424.

When did DCG-VII ELECTROCARDIOSCANNER receive FDA 510(k) clearance?

DCG-VII ELECTROCARDIOSCANNER received FDA 510(k) clearance on 1979-08-28, under 510(k) number K791424.

Who is the listed applicant for DCG-VII ELECTROCARDIOSCANNER?

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

What is the FDA product code for DCG-VII ELECTROCARDIOSCANNER?

The FDA product code for DCG-VII ELECTROCARDIOSCANNER is DSI.

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 Del Mar Avionics 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 54 devices →

Related Devices (Code: DSI)

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

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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