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FDA 510(k)

CPR RSQ ASSIST

K-Number: K123248 · 2013-12-10

ApplicantAvantech, Inc.
Decision Date2013-12-10
Product CodeLIX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPR RSQ ASSIST is the device name listed in this FDA 510(k) record. The listed applicant is Avantech, Inc.. It received FDA 510(k) clearance on 2013-12-10 under 510(k) number K123248. 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 RSQ ASSIST?

CPR RSQ ASSIST is a medical device that received FDA 510(k) clearance on 2013-12-10. The listed applicant is Avantech, Inc.. The 510(k) number is K123248.

When did CPR RSQ ASSIST receive FDA 510(k) clearance?

CPR RSQ ASSIST received FDA 510(k) clearance on 2013-12-10, under 510(k) number K123248.

Who is the listed applicant for CPR RSQ ASSIST?

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

What is the FDA product code for CPR RSQ ASSIST?

The FDA product code for CPR RSQ ASSIST 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 ASK123597TRUECPR COACHING DEVICEPhysio-Control, Inc.K122050CPRMETER CPR FEEDBACK DEVICELaerdal Medical A/SK112660POCKETCPRZoll 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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