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FDA 510(k), K173224, SPIN-SWI
FDA 510(k), K173224, SPIN-SWI
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510(K) Number: K173224
Device Name: SPIN-SWI
Manufacturer: SpinTech, Inc.
Device Classification Name: system, nuclear magnetic resonance imaging
Regulation Number: 892.1000
Classification Product Code: LNH
Date Received: 10/03/2017
Decision Date: 02/23/2018
Regulation Medical Specialty: Radiology
Device Name: SPIN-SWI
Manufacturer: SpinTech, Inc.
Device Classification Name: system, nuclear magnetic resonance imaging
Regulation Number: 892.1000
Classification Product Code: LNH
Date Received: 10/03/2017
Decision Date: 02/23/2018
Regulation Medical Specialty: Radiology
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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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