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FDA 510(k)

ENERTRON CPR JACK

K-Number: K024215 · 2004-05-14

ApplicantEnertron Engineering Co.
Decision Date2004-05-14
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENERTRON CPR JACK is the device name listed in this FDA 510(k) record. The listed applicant is Enertron Engineering Co.. It received FDA 510(k) clearance on 2004-05-14 under 510(k) number K024215. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENERTRON CPR JACK?

ENERTRON CPR JACK is a medical device that received FDA 510(k) clearance on 2004-05-14. The listed applicant is Enertron Engineering Co.. The 510(k) number is K024215.

When did ENERTRON CPR JACK receive FDA 510(k) clearance?

ENERTRON CPR JACK received FDA 510(k) clearance on 2004-05-14, under 510(k) number K024215.

Who is the listed applicant for ENERTRON CPR JACK?

The FDA 510(k) record lists Enertron Engineering Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENERTRON CPR JACK?

The FDA product code for ENERTRON CPR JACK is DRM.

Related Clinical Trials

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Related Devices (Code: DRM)

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.

K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLCK173553LUCAS 3 Chest Compression SystemJolife ABK161768LUCAS 3 Chest Compression SystemJolife ABK153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLCK112998AUTOPULSE RESUSCITATION SYSTEM MODEL 1000Zoll Circulation

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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