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FDA 510(k), K093160, HEADWAY 21 MICROCATHETER, MODEL: MC212150S
FDA 510(k), K093160, HEADWAY 21 MICROCATHETER, MODEL: MC212150S
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510(K) Number: K093160
Device Name: HEADWAY 21 MICROCATHETER, MODEL: MC212150S
Manufacturer: MICROVENTION, INC.
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 10/06/2009
Decision Date: 11/05/2009
Regulation Medical Specialty: Cardiovascular
Device Name: HEADWAY 21 MICROCATHETER, MODEL: MC212150S
Manufacturer: MICROVENTION, INC.
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 10/06/2009
Decision Date: 11/05/2009
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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