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FDA 510(k), K212896, Visible Patient Suite
FDA 510(k), K212896, Visible Patient Suite
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$149.00 USD
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510(K) Number: K212896
Device Name: Visible Patient Suite
Manufacturer: Visible Patient, SAS
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 09/10/2021
Decision Date: 11/05/2021
Regulation Medical Specialty: Radiology
Device Name: Visible Patient Suite
Manufacturer: Visible Patient, SAS
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 09/10/2021
Decision Date: 11/05/2021
Regulation Medical Specialty: Radiology
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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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