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FDA 510(k), K121171, CUROS TIP
FDA 510(k), K121171, CUROS TIP
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$149.00 USD
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510(K) Number: K121171
Device Name: CUROS TIP
Manufacturer: IVERA MEDICAL, INC.
Device Classification Name: cap, device disinfectant
Regulation Number: 880.5440
Classification Product Code: QBP
Date Received: 04/17/2012
Decision Date: 11/26/2012
Regulation Medical Specialty: General Hospital
Device Name: CUROS TIP
Manufacturer: IVERA MEDICAL, INC.
Device Classification Name: cap, device disinfectant
Regulation Number: 880.5440
Classification Product Code: QBP
Date Received: 04/17/2012
Decision Date: 11/26/2012
Regulation Medical Specialty: General Hospital
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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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