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FDA 510(k)

LUCAS 3 Chest Compression System

K-Number: K173553 · 2018-02-08

ApplicantJolife AB
Decision Date2018-02-08
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LUCAS 3 Chest Compression System is a medical device manufactured by Jolife AB. It received FDA 510(k) clearance on 2018-02-08 under approval number K173553. 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 LUCAS 3 Chest Compression System?

LUCAS 3 Chest Compression System is a medical device that received FDA 510(k) clearance on 2018-02-08. It is manufactured by Jolife AB. The 510(k) number is K173553.

When was LUCAS 3 Chest Compression System approved by the FDA?

LUCAS 3 Chest Compression System received FDA 510(k) clearance on 2018-02-08, under approval number K173553.

What company makes LUCAS 3 Chest Compression System?

LUCAS 3 Chest Compression System is manufactured by Jolife AB.

What is the FDA product code for LUCAS 3 Chest Compression System?

The FDA product code for LUCAS 3 Chest Compression System is DRM.

Related Clinical Trials

NCT01143454 Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System RECRUITING NCT03331380 Technical Development of Cardiovascular Magnetic Resonance Imaging (CMR) Using a Low Specific Absorption Rate (SAR) Scanner System RECRUITING NCT07609511 Magnet System Gastric Outlet Obstruction Study NOT_YET_RECRUITING NCT07603531 Assessment of the Efficacy of the Dynamic Decongestive System in the Maintenance Phase of Lower Limb Lymphedema NOT_YET_RECRUITING NCT07373496 Patient Position Monitoring System for Beam Gated Radiation Therapy of Malignancies of the Chest and Upper Abdomen RECRUITING NCT07600489 A Randomized Non-Inferiority Study of Mepi™ Press 2 vs UrgoK2® for Compression Therapy in Venous Leg Ulcers NOT_YET_RECRUITING

Other Devices by Jolife AB

K161768LUCAS 3 Chest Compression System

Related Devices (Code: DRM)

K161768LUCAS 3 Chest Compression SystemJolife AB K153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLC K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLC K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.

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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