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FDA 510(k), K161768, LUCAS 3 Chest Compression System
FDA 510(k), K161768, LUCAS 3 Chest Compression System
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510(K) Number: K161768
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: 06/27/2016
Decision Date: 11/09/2016
Regulation Medical Specialty: Cardiovascular
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: 06/27/2016
Decision Date: 11/09/2016
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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