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FDA 510(k)

ACUTE CARDIAC CARE SYSTEM

K-Number: K772006 · 1977-11-28

ApplicantPhysio-Control Corp.
Decision Date1977-11-28
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACUTE CARDIAC CARE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1977-11-28 under 510(k) number K772006. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUTE CARDIAC CARE SYSTEM?

ACUTE CARDIAC CARE SYSTEM is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Physio-Control Corp.. The 510(k) number is K772006.

When did ACUTE CARDIAC CARE SYSTEM receive FDA 510(k) clearance?

ACUTE CARDIAC CARE SYSTEM received FDA 510(k) clearance on 1977-11-28, under 510(k) number K772006.

Who is the listed applicant for ACUTE CARDIAC CARE SYSTEM?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUTE CARDIAC CARE SYSTEM?

The FDA product code for ACUTE CARDIAC CARE SYSTEM is DRT.

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Other records listing Physio-Control Corp. as applicant

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Related Devices (Code: DRT)

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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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