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FDA 510(k), K202527, Zio ECG Utilization Software (ZEUS) System
FDA 510(k), K202527, Zio ECG Utilization Software (ZEUS) System
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$149.00 USD
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510(K) Number: K202527
Device Name: Zio ECG Utilization Software (ZEUS) System
Manufacturer: Gabrielle Logan
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: DQK
Classification Product Code: 09/01/2020
Date Received: 05/21/2021
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: Zio ECG Utilization Software (ZEUS) System
Manufacturer: Gabrielle Logan
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: DQK
Classification Product Code: 09/01/2020
Date Received: 05/21/2021
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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