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FDA 510(k)

CPR LOCATOR

K-Number: K833737 · 1984-08-24

ApplicantLifepoint,Inc
Decision Date1984-08-24
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPR LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Lifepoint,Inc. It received FDA 510(k) clearance on 1984-08-24 under 510(k) number K833737. The device is classified under product code LIX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR LOCATOR?

CPR LOCATOR is a medical device that received FDA 510(k) clearance on 1984-08-24. The listed applicant is Lifepoint,Inc. The 510(k) number is K833737.

When did CPR LOCATOR receive FDA 510(k) clearance?

CPR LOCATOR received FDA 510(k) clearance on 1984-08-24, under 510(k) number K833737.

Who is the listed applicant for CPR LOCATOR?

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

What is the FDA product code for CPR LOCATOR?

The FDA product code for CPR LOCATOR is LIX.

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Other records listing Lifepoint,Inc 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.

K041747IMPACT TEST SYSTEM SALIVA TEST MODULE-OPIATE (WORKPLACE)K041746IMPACT TEST SYSTEM; SALIVA TEST MODULE-OPIATE (PRESCRIPTION USE)

Related Devices (Code: LIX)

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.

K201581CPR BANDCredoK183348Reusable Silicone Cover CPRmeter 2Laerdal Medical ASK173886CPRmeter 2 CPR Feedback DeviceLaerdal Medical ASK123248CPR RSQ ASSISTAvantech, Inc.K123597TRUECPR COACHING DEVICEPhysio-Control, Inc.K122050CPRMETER CPR FEEDBACK DEVICELaerdal Medical A/S

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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