FDA 510(k), K182456, Study Watch
FDA 510(k), K182456, Study Watch
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510(K) Number: K182456
Device Name: Study Watch
Manufacturer: Verily Life Sciences LLC
Device Classification Name: transmitters and receivers, electrocardiograph, telephone
Regulation Number: 870.2920
Classification Product Code: DXH
Date Received: 09/07/2018
Decision Date: 01/17/2019
Regulation Medical Specialty: Cardiovascular
Device Name: Study Watch
Manufacturer: Verily Life Sciences LLC
Device Classification Name: transmitters and receivers, electrocardiograph, telephone
Regulation Number: 870.2920
Classification Product Code: DXH
Date Received: 09/07/2018
Decision Date: 01/17/2019
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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