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FDA 510(k), K001773, ORTHONE
FDA 510(k), K001773, ORTHONE
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510(K) Number: K001773
Device Name: ORTHONE
Manufacturer: MICHAEL A DOUGLAS
Device Classification Name: System, Nuclear Magnetic Resonance Imaging
Regulation Number: LNH
Classification Product Code: 06/12/2000
Date Received: 08/18/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: ORTHONE
Manufacturer: MICHAEL A DOUGLAS
Device Classification Name: System, Nuclear Magnetic Resonance Imaging
Regulation Number: LNH
Classification Product Code: 06/12/2000
Date Received: 08/18/2000
Decision Date: Substantially Equivalent (SESE)
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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