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FDA 510(k)

CARDIAC OUTPUT MODULE-78231C

K-Number: K772234 · 1978-01-05

Decision Date1978-01-05
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIAC OUTPUT MODULE-78231C 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 1978-01-05 under 510(k) number K772234. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIAC OUTPUT MODULE-78231C?

CARDIAC OUTPUT MODULE-78231C is a medical device that received FDA 510(k) clearance on 1978-01-05. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K772234.

When did CARDIAC OUTPUT MODULE-78231C receive FDA 510(k) clearance?

CARDIAC OUTPUT MODULE-78231C received FDA 510(k) clearance on 1978-01-05, under 510(k) number K772234.

Who is the listed applicant for CARDIAC OUTPUT MODULE-78231C?

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 CARDIAC OUTPUT MODULE-78231C?

The FDA product code for CARDIAC OUTPUT MODULE-78231C is DSK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Hewlett-Packard Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 230 devices →

Related Devices (Code: DSK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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