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FDA 510(k), K143304, Sickbay Clinical Platform
FDA 510(k), K143304, Sickbay Clinical Platform
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510(K) Number: K143304
Device Name: Sickbay Clinical Platform
Manufacturer: Ralph Krog
Device Classification Name: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Regulation Number: MWI
Classification Product Code: 11/18/2014
Date Received: 05/26/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: Sickbay Clinical Platform
Manufacturer: Ralph Krog
Device Classification Name: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Regulation Number: MWI
Classification Product Code: 11/18/2014
Date Received: 05/26/2015
Decision Date: Substantially Equivalent (SESE)
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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