FDA 510(k), K990560, LIFE IMAGING SYSTEMS, MODEL L3DI
FDA 510(k), K990560, LIFE IMAGING SYSTEMS, MODEL L3DI
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510(K) Number: K990560
Device Name: LIFE IMAGING SYSTEMS, MODEL L3DI
Manufacturer:
Device Classification Name: System, Imaging, Pulsed Echo, Ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 02/22/1999
Decision Date: 05/20/1999
Regulation Medical Specialty: Radiology
Device Name: LIFE IMAGING SYSTEMS, MODEL L3DI
Manufacturer:
Device Classification Name: System, Imaging, Pulsed Echo, Ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 02/22/1999
Decision Date: 05/20/1999
Regulation Medical Specialty: Radiology