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FDA 510(k)

CPR PROMPT

K-Number: K954692 · 1996-03-27

ApplicantCounty Line , Ltd.
Decision Date1996-03-27
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPR PROMPT is the device name listed in this FDA 510(k) record. The listed applicant is County Line , Ltd.. It received FDA 510(k) clearance on 1996-03-27 under 510(k) number K954692. 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 PROMPT?

CPR PROMPT is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is County Line , Ltd.. The 510(k) number is K954692.

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

CPR PROMPT received FDA 510(k) clearance on 1996-03-27, under 510(k) number K954692.

Who is the listed applicant for CPR PROMPT?

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

What is the FDA product code for CPR PROMPT?

The FDA product code for CPR PROMPT is LIX.

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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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