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FDA 510(k)

DCG DATA TERMINAL

K-Number: K792071 · 1979-12-04

ApplicantDel Mar Avionics
Decision Date1979-12-04
Product Code
DecisionSubstantially Equivalent

Device Summary

DCG DATA TERMINAL 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 1979-12-04 under 510(k) number K792071. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DCG DATA TERMINAL?

DCG DATA TERMINAL is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is Del Mar Avionics. The 510(k) number is K792071.

When did DCG DATA TERMINAL receive FDA 510(k) clearance?

DCG DATA TERMINAL received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792071.

Who is the listed applicant for DCG DATA TERMINAL?

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

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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.

K990027OMNICORDER, MODEL 464K971696SENTINEL RECORDER, MODELS 471/472K963174HOLTER DIGICORDER WITH PACER OPTION (MODEL 483)K950020HOLTER PACERCORDER(R)K942653HOLTER SSR DIGICORDER(TM)K922221SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM

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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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