FDA 510(k), K891180, TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT

FDA 510(k), K891180, TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT

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510(K) Number: K891180
Device Name: TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT
Manufacturer: INGRESS TECHNOLOGIES, INC.
Device Classification Name: transducer, vessel occlusion
Regulation Number: 870.2890
Classification Product Code: DXP
Date Received: 03/06/1989
Decision Date: 06/15/1989
Regulation Medical Specialty: Cardiovascular

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