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
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
- 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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