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FDA 510(k), K110826, CUROS PORT PROTECTOR
FDA 510(k), K110826, CUROS PORT PROTECTOR
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510(K) Number: K110826
Device Name: CUROS PORT PROTECTOR
Manufacturer: DON CANAL
Device Classification Name: Cap, Device Disinfectant
Regulation Number: QBP
Classification Product Code: KXA
Date Received: 03/24/2011
Decision Date: 06/23/2011
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: CUROS PORT PROTECTOR
Manufacturer: DON CANAL
Device Classification Name: Cap, Device Disinfectant
Regulation Number: QBP
Classification Product Code: KXA
Date Received: 03/24/2011
Decision Date: 06/23/2011
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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