FDA 510(k), K183078, VitalConnect Platform, VitalPatch Biosensor
FDA 510(k), K183078, VitalConnect Platform, VitalPatch Biosensor
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510(K) Number: K183078
Device Name: VitalConnect Platform, VitalPatch Biosensor
Manufacturer: VitalConnect, Inc.
Device Classification Name: Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 11/05/2018
Decision Date: 03/07/2019
Regulation Medical Specialty: Cardiovascular
Device Name: VitalConnect Platform, VitalPatch Biosensor
Manufacturer: VitalConnect, Inc.
Device Classification Name: Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation Number: 870.2910
Classification Product Code: DRG
Date Received: 11/05/2018
Decision Date: 03/07/2019
Regulation Medical Specialty: Cardiovascular
- 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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