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FDA 510(k), K033960, OLINDA/EXM
FDA 510(k), K033960, OLINDA/EXM
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510(K) Number: K033960
Device Name: OLINDA/EXM
Manufacturer: VANDERBILT UNIVERSITY
Device Classification Name: Camera, Scintillation (Gamma)
Regulation Number: 892.1100
Classification Product Code: IYX
Date Received: 12/22/2003
Decision Date: 06/15/2004
Regulation Medical Specialty: Radiology
Device Name: OLINDA/EXM
Manufacturer: VANDERBILT UNIVERSITY
Device Classification Name: Camera, Scintillation (Gamma)
Regulation Number: 892.1100
Classification Product Code: IYX
Date Received: 12/22/2003
Decision Date: 06/15/2004
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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