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FDA 510(k)

MODEL 78231D CARDIAC OUTPUT MODULE

K-Number: K850568 · 1985-04-09

ApplicantHewlett-Packard Co.
Decision Date1985-04-09
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 78231D CARDIAC OUTPUT MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1985-04-09 under 510(k) number K850568. 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 78231D CARDIAC OUTPUT MODULE?

MODEL 78231D CARDIAC OUTPUT MODULE is a medical device that received FDA 510(k) clearance on 1985-04-09. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K850568.

When did MODEL 78231D CARDIAC OUTPUT MODULE receive FDA 510(k) clearance?

MODEL 78231D CARDIAC OUTPUT MODULE received FDA 510(k) clearance on 1985-04-09, under 510(k) number K850568.

Who is the listed applicant for MODEL 78231D CARDIAC OUTPUT MODULE?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 78231D CARDIAC OUTPUT MODULE?

The FDA product code for MODEL 78231D CARDIAC OUTPUT MODULE is DXG.

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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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