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FDA 510(k)

PACE AID

K-Number: K811028 · 1981-04-16

ApplicantCardiac Resucitator Corp.
Decision Date1981-04-16
Product Code
DecisionUnknown

Device Summary

PACE AID is the device name listed in this FDA 510(k) record. The listed applicant is Cardiac Resucitator Corp.. It received FDA 510(k) clearance on 1981-04-16 under 510(k) number K811028. FDA Decision: Unknown.

Frequently Asked Questions

What is the PACE AID?

PACE AID is a medical device that received FDA 510(k) clearance on 1981-04-16. The listed applicant is Cardiac Resucitator Corp.. The 510(k) number is K811028.

When did PACE AID receive FDA 510(k) clearance?

PACE AID received FDA 510(k) clearance on 1981-04-16, under 510(k) number K811028.

Who is the listed applicant for PACE AID?

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

Other records listing Cardiac Resucitator Corp. 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.

K882513MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORK871538STAT-PAD (TM)K871971MODIFIED PACE*AID MODEL 53K871569MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORK870622HEART*AID 1000K850596PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &

View all 17 devices →

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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