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FDA 510(k), K172258, Novasight Hybrid System
FDA 510(k), K172258, Novasight Hybrid System
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$149.00 USD
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510(K) Number: K172258
Device Name: Novasight Hybrid System
Manufacturer: Conavi Medical Inc.
Device Classification Name: catheter, ultrasound, intravascular
Regulation Number: 870.1200
Classification Product Code: OBJ
Date Received: 07/26/2017
Decision Date: 04/27/2018
Regulation Medical Specialty: Cardiovascular
Device Name: Novasight Hybrid System
Manufacturer: Conavi Medical Inc.
Device Classification Name: catheter, ultrasound, intravascular
Regulation Number: 870.1200
Classification Product Code: OBJ
Date Received: 07/26/2017
Decision Date: 04/27/2018
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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