FDA 510(k)

CARDIAC OUTPUT COMPUTER

K-Number: K760600 · 1976-10-15

ApplicantCardiopulmonary Instrumentation

Decision Date1976-10-15

Product CodeDXG

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CARDIAC OUTPUT COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Cardiopulmonary Instrumentation. It received FDA 510(k) clearance on 1976-10-15 under 510(k) number K760600. 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 CARDIAC OUTPUT COMPUTER?

CARDIAC OUTPUT COMPUTER is a medical device that received FDA 510(k) clearance on 1976-10-15. The listed applicant is Cardiopulmonary Instrumentation. The 510(k) number is K760600.

When did CARDIAC OUTPUT COMPUTER receive FDA 510(k) clearance?

CARDIAC OUTPUT COMPUTER received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760600.

Who is the listed applicant for CARDIAC OUTPUT COMPUTER?

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

What is the FDA product code for CARDIAC OUTPUT COMPUTER?

The FDA product code for CARDIAC OUTPUT COMPUTER is DXG.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.