FDA 510(k), K150831, Cellvizio 100 Series System with Confocal Miniprobes
FDA 510(k), K150831, Cellvizio 100 Series System with Confocal Miniprobes
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510(K) Number: K150831
Device Name: Cellvizio 100 Series System with Confocal Miniprobes
Manufacturer: MAUNA KEA TECHNOLOGIES
Device Classification Name: confocal optical imaging
Regulation Number: 876.1500
Classification Product Code: OWN
Date Received: 03/30/2015
Decision Date: 12/22/2015
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: Cellvizio 100 Series System with Confocal Miniprobes
Manufacturer: MAUNA KEA TECHNOLOGIES
Device Classification Name: confocal optical imaging
Regulation Number: 876.1500
Classification Product Code: OWN
Date Received: 03/30/2015
Decision Date: 12/22/2015
Regulation Medical Specialty: Gastroenterology/Urology
- 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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