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FDA 510(k)

MODEL 1979 BLOOD PRESSUROMETER R CHARTER

K-Number: K792073 · 1979-11-05

ApplicantDel Mar Avionics
Decision Date1979-11-05
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 1979 BLOOD PRESSUROMETER R CHARTER 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 1979-11-05 under 510(k) number K792073. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1979 BLOOD PRESSUROMETER R CHARTER?

MODEL 1979 BLOOD PRESSUROMETER R CHARTER is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Del Mar Avionics. The 510(k) number is K792073.

When did MODEL 1979 BLOOD PRESSUROMETER R CHARTER receive FDA 510(k) clearance?

MODEL 1979 BLOOD PRESSUROMETER R CHARTER received FDA 510(k) clearance on 1979-11-05, under 510(k) number K792073.

Who is the listed applicant for MODEL 1979 BLOOD PRESSUROMETER R CHARTER?

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 1979 BLOOD PRESSUROMETER R CHARTER?

The FDA product code for MODEL 1979 BLOOD PRESSUROMETER R CHARTER is DRS.

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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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