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FDA 510(k), K103411, IDEAL IQ SOFTWARE OPTION
FDA 510(k), K103411, IDEAL IQ SOFTWARE OPTION
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510(K) Number: K103411
Device Name: IDEAL IQ SOFTWARE OPTION
Manufacturer: GE MEDICAL SYSTEMS
Device Classification Name: System, Nuclear Magnetic Resonance Imaging
Regulation Number: 892.1000
Classification Product Code: LNH
Date Received: 11/22/2010
Decision Date: 03/22/2011
Regulation Medical Specialty: Radiology
Device Name: IDEAL IQ SOFTWARE OPTION
Manufacturer: GE MEDICAL SYSTEMS
Device Classification Name: System, Nuclear Magnetic Resonance Imaging
Regulation Number: 892.1000
Classification Product Code: LNH
Date Received: 11/22/2010
Decision Date: 03/22/2011
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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