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FDA 510(k), K102365, MICROPLEX COIL SYSTEM- COSMOS
FDA 510(k), K102365, MICROPLEX COIL SYSTEM- COSMOS
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510(K) Number: K102365
Device Name: MICROPLEX COIL SYSTEM- COSMOS
Manufacturer: MICROVENTION, INC.
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 08/20/2010
Decision Date: 11/18/2010
Regulation Medical Specialty: Cardiovascular
Device Name: MICROPLEX COIL SYSTEM- COSMOS
Manufacturer: MICROVENTION, INC.
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 08/20/2010
Decision Date: 11/18/2010
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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