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FDA 510(k)

HEART - AID ALS, 95

K-Number: K841556 · 1984-07-19

ApplicantCardiac Resucitator Corp.
Decision Date1984-07-19
Product CodeLDO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

HEART - AID ALS, 95 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 1984-07-19 under 510(k) number K841556. The device is classified under product code LDO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEART - AID ALS, 95?

HEART - AID ALS, 95 is a medical device that received FDA 510(k) clearance on 1984-07-19. The listed applicant is Cardiac Resucitator Corp.. The 510(k) number is K841556.

When did HEART - AID ALS, 95 receive FDA 510(k) clearance?

HEART - AID ALS, 95 received FDA 510(k) clearance on 1984-07-19, under 510(k) number K841556.

Who is the listed applicant for HEART - AID ALS, 95?

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

What is the FDA product code for HEART - AID ALS, 95?

The FDA product code for HEART - AID ALS, 95 is LDO.

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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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