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FDA 510(k), K171056, WAVE Clinical Platform
FDA 510(k), K171056, WAVE Clinical Platform
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510(K) Number: K171056
Device Name: WAVE Clinical Platform
Manufacturer: Lance Burton
Device Classification Name: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Regulation Number: MWI
Classification Product Code: 04/10/2017
Date Received: 01/04/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: WAVE Clinical Platform
Manufacturer: Lance Burton
Device Classification Name: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Regulation Number: MWI
Classification Product Code: 04/10/2017
Date Received: 01/04/2018
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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