• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K173553, LUCAS 3 Chest Compression System, by Jolife AB

FDA 510(k) K173553, LUCAS 3 Chest Compression System, by Jolife AB

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510(K) Number: K173553
Device Name: LUCAS 3 Chest Compression System
Manufacturer: Jolife AB
Device Classification Name: compressor, cardiac, external
Regulation Number: 870.5200
Classification Product Code: DRM
Date Received: 11/16/2017
Decision Date: 02/08/2018
Regulation Medical Specialty: Cardiovascular
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