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FDA 510(k)

MODEL 656 ARRHYTHMIA ANALYZER

K-Number: K792080 · 1979-12-04

ApplicantDel Mar Avionics
Decision Date1979-12-04
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 656 ARRHYTHMIA ANALYZER 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 K792080. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 656 ARRHYTHMIA ANALYZER?

MODEL 656 ARRHYTHMIA ANALYZER 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 K792080.

When did MODEL 656 ARRHYTHMIA ANALYZER receive FDA 510(k) clearance?

MODEL 656 ARRHYTHMIA ANALYZER received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792080.

Who is the listed applicant for MODEL 656 ARRHYTHMIA ANALYZER?

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 MODEL 656 ARRHYTHMIA ANALYZER?

The FDA product code for MODEL 656 ARRHYTHMIA ANALYZER is DXG.

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Other records listing Del Mar Avionics as applicant

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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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