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FDA 510(k), K140557, MIVI 6F GUIDE CATHETER
FDA 510(k), K140557, MIVI 6F GUIDE CATHETER
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$149.00 USD
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510(K) Number: K140557
Device Name: MIVI 6F GUIDE CATHETER
Manufacturer: MIVI, LLC
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 03/05/2014
Decision Date: 09/18/2014
Regulation Medical Specialty: Cardiovascular
Device Name: MIVI 6F GUIDE CATHETER
Manufacturer: MIVI, LLC
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 03/05/2014
Decision Date: 09/18/2014
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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