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FDA 510(k)

MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH

K-Number: K872658 · 1988-01-06

ApplicantDel Mar Avionics
Decision Date1988-01-06
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH 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 1988-01-06 under 510(k) number K872658. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH?

MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Del Mar Avionics. The 510(k) number is K872658.

When did MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH receive FDA 510(k) clearance?

MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH received FDA 510(k) clearance on 1988-01-06, under 510(k) number K872658.

Who is the listed applicant for MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH?

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 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH?

The FDA product code for MODEL 980-CARDIOSCOPE AT-3 ELECTROCARDIOGRAPH is DPS.

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Other records listing Del Mar Avionics as applicant

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Related Devices (Code: DPS)

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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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