DCG-VII ELECTROCARDIOSCANNER
K-Number: K791424 · 1979-08-28
Advertisement
Device Summary
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.
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.
Advertisement