FDA 510(k)

CPR EZY MASK AND PAD

K-Number: K003937 · 2001-06-06

Decision Date2001-06-06

Product CodeLIX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CPR EZY MASK AND PAD is the device name listed in this FDA 510(k) record. The listed applicant is Medteq Innovations Pty, Ltd.. It received FDA 510(k) clearance on 2001-06-06 under 510(k) number K003937. 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 EZY MASK AND PAD?

CPR EZY MASK AND PAD is a medical device that received FDA 510(k) clearance on 2001-06-06. The listed applicant is Medteq Innovations Pty, Ltd.. The 510(k) number is K003937.

When did CPR EZY MASK AND PAD receive FDA 510(k) clearance?

CPR EZY MASK AND PAD received FDA 510(k) clearance on 2001-06-06, under 510(k) number K003937.

Who is the listed applicant for CPR EZY MASK AND PAD?

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

What is the FDA product code for CPR EZY MASK AND PAD?

The FDA product code for CPR EZY MASK AND PAD is LIX.

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 BANDCredo K183348Reusable Silicone Cover CPRmeter 2Laerdal Medical AS K173886CPRmeter 2 CPR Feedback DeviceLaerdal Medical AS K123248CPR 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.