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FDA 510(k)

CPRMETER CPR FEEDBACK DEVICE

K-Number: K122050 · 2012-10-22

ApplicantLaerdal Medical A/S
Decision Date2012-10-22
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPRMETER CPR FEEDBACK DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Laerdal Medical A/S. It received FDA 510(k) clearance on 2012-10-22 under 510(k) number K122050. 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 CPR FEEDBACK DEVICE?

CPRMETER CPR FEEDBACK DEVICE is a medical device that received FDA 510(k) clearance on 2012-10-22. The listed applicant is Laerdal Medical A/S. The 510(k) number is K122050.

When did CPRMETER CPR FEEDBACK DEVICE receive FDA 510(k) clearance?

CPRMETER CPR FEEDBACK DEVICE received FDA 510(k) clearance on 2012-10-22, under 510(k) number K122050.

Who is the listed applicant for CPRMETER CPR FEEDBACK DEVICE?

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

What is the FDA product code for CPRMETER CPR FEEDBACK DEVICE?

The FDA product code for CPRMETER CPR FEEDBACK DEVICE is LIX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Laerdal Medical A/S 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.

K023805LAERDAL PAEDIATRIC POCKET MASK, MODEL 820050K993668LAERDAL SUCTION UNIT,(4000) MODEL 78 00 20

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.K112660POCKETCPRZoll Medical Corp

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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