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FDA 510(k)

CPRmeter 2 CPR Feedback Device

K-Number: K173886 · 2018-03-23

ApplicantLaerdal Medical AS
Decision Date2018-03-23
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPRmeter 2 CPR Feedback Device is a medical device manufactured by Laerdal Medical AS. It received FDA 510(k) clearance on 2018-03-23 under approval number K173886. 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 CPRmeter 2 CPR Feedback Device?

CPRmeter 2 CPR Feedback Device is a medical device that received FDA 510(k) clearance on 2018-03-23. It is manufactured by Laerdal Medical AS. The 510(k) number is K173886.

When was CPRmeter 2 CPR Feedback Device approved by the FDA?

CPRmeter 2 CPR Feedback Device received FDA 510(k) clearance on 2018-03-23, under approval number K173886.

What company makes CPRmeter 2 CPR Feedback Device?

CPRmeter 2 CPR Feedback Device is manufactured by Laerdal Medical AS.

What is the FDA product code for CPRmeter 2 CPR Feedback Device?

The FDA product code for CPRmeter 2 CPR Feedback Device is LIX.

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Other Devices by Laerdal Medical AS

K183348Reusable Silicone Cover CPRmeter 2 K232111NeoBeat, NeoBeat Mini K251631The BAG manual resuscitator and accessories

Related Devices (Code: LIX)

K183348Reusable Silicone Cover CPRmeter 2Laerdal Medical AS K201581CPR BANDCredo

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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