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FDA 510(k), K190176, MINAMO
FDA 510(k), K190176, MINAMO
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$149.00 USD
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510(K) Number: K190176
Device Name: MINAMO
Manufacturer: Asahi Intecc Co., Ltd.
Device Classification Name: wire, guide, catheter
Regulation Number: 870.1330
Classification Product Code: DQX
Date Received: 02/01/2019
Decision Date: 08/01/2019
Regulation Medical Specialty: Cardiovascular
Device Name: MINAMO
Manufacturer: Asahi Intecc Co., Ltd.
Device Classification Name: wire, guide, catheter
Regulation Number: 870.1330
Classification Product Code: DQX
Date Received: 02/01/2019
Decision Date: 08/01/2019
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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