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FDA 510(k), K131305, CHISON DIAGNOSTIC ULTRASOUND SYSTEM, CONVEX PROBE, LINCAR PROBE, PHASED PROBE
FDA 510(k), K131305, CHISON DIAGNOSTIC ULTRASOUND SYSTEM, CONVEX PROBE, LINCAR PROBE, PHASED PROBE
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510(K) Number: K131305
Device Name: CHISON DIAGNOSTIC ULTRASOUND SYSTEM, CONVEX PROBE, LINCAR PROBE, PHASED PROBE
Manufacturer: CHISON MEDICAL IMAGING CO., LTD.
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 05/07/2013
Decision Date: 08/01/2013
Regulation Medical Specialty: Radiology
Device Name: CHISON DIAGNOSTIC ULTRASOUND SYSTEM, CONVEX PROBE, LINCAR PROBE, PHASED PROBE
Manufacturer: CHISON MEDICAL IMAGING CO., LTD.
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 05/07/2013
Decision Date: 08/01/2013
Regulation Medical Specialty: Radiology
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