FDA 510(k)

CPRmeter 2 CPR Feedback Device

K-Number: K173886 · 2018-03-23

Decision Date2018-03-23

Product CodeLIX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CPRmeter 2 CPR Feedback Device is the device name listed in this FDA 510(k) record. The listed applicant is Laerdal Medical AS. It received FDA 510(k) clearance on 2018-03-23 under 510(k) 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. The listed applicant is Laerdal Medical AS. The 510(k) number is K173886.

When did CPRmeter 2 CPR Feedback Device receive FDA 510(k) clearance?

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

Who is the listed applicant for CPRmeter 2 CPR Feedback Device?

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

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

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

Other records listing Laerdal Medical AS 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.

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

Related Devices (Code: LIX)

K201581CPR BANDCredo K183348Reusable Silicone Cover CPRmeter 2Laerdal Medical AS

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.