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FDA 510(k), K052293, GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM
FDA 510(k), K052293, GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM
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510(K) Number: K052293
Device Name: GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM
Manufacturer: LARRY A KROGER, PH.D.
Device Classification Name: System, Nuclear Magnetic Resonance Imaging
Regulation Number: LNH
Classification Product Code: 08/23/2005
Date Received: 09/21/2005
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM
Manufacturer: LARRY A KROGER, PH.D.
Device Classification Name: System, Nuclear Magnetic Resonance Imaging
Regulation Number: LNH
Classification Product Code: 08/23/2005
Date Received: 09/21/2005
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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