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FDA 510(k), K103730, GE LUNAR VISCERAL FAT SOFTWARE
FDA 510(k), K103730, GE LUNAR VISCERAL FAT SOFTWARE
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510(K) Number: K103730
Device Name: GE LUNAR VISCERAL FAT SOFTWARE
Manufacturer: GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Device Classification Name: densitometer, bone
Regulation Number: 892.1170
Classification Product Code: KGI
Date Received: 12/21/2010
Decision Date: 05/06/2011
Regulation Medical Specialty: Radiology
Device Name: GE LUNAR VISCERAL FAT SOFTWARE
Manufacturer: GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Device Classification Name: densitometer, bone
Regulation Number: 892.1170
Classification Product Code: KGI
Date Received: 12/21/2010
Decision Date: 05/06/2011
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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