FDA 510(k), K140657, CUROS RED PORT PROTECTOR
FDA 510(k), K140657, CUROS RED PORT PROTECTOR
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510(K) Number: K140657
Device Name: CUROS RED PORT PROTECTOR
Manufacturer: IVERA MEDICAL, INC.
Device Classification Name: cap, device disinfectant
Regulation Number: 880.5440
Classification Product Code: QBP
Date Received: 03/14/2014
Decision Date: 12/04/2014
Regulation Medical Specialty: General Hospital
Device Name: CUROS RED PORT PROTECTOR
Manufacturer: IVERA MEDICAL, INC.
Device Classification Name: cap, device disinfectant
Regulation Number: 880.5440
Classification Product Code: QBP
Date Received: 03/14/2014
Decision Date: 12/04/2014
Regulation Medical Specialty: General Hospital
- 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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