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FDA 510(k)

CPR HEARTSAVER AND BREATHOLATOR

K-Number: K831198 · 1983-06-24

ApplicantCervco Corp.
Decision Date1983-06-24
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CPR HEARTSAVER AND BREATHOLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cervco Corp.. It received FDA 510(k) clearance on 1983-06-24 under 510(k) number K831198. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR HEARTSAVER AND BREATHOLATOR?

CPR HEARTSAVER AND BREATHOLATOR is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Cervco Corp.. The 510(k) number is K831198.

When did CPR HEARTSAVER AND BREATHOLATOR receive FDA 510(k) clearance?

CPR HEARTSAVER AND BREATHOLATOR received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831198.

Who is the listed applicant for CPR HEARTSAVER AND BREATHOLATOR?

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

What is the FDA product code for CPR HEARTSAVER AND BREATHOLATOR?

The FDA product code for CPR HEARTSAVER AND BREATHOLATOR is BTM.

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.

Related Devices (Code: BTM)

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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