Atl Ultrasound, Inc. is one of 25749 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atl Ultrasound, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HDI 5000 ULTRASOUND SYSTEM WITH EXTENDED FIELD OF VIEW IMAGING, HDI 1500/SA 8800 ULTRASOUND SYSTEM WITH MULTIPLANE TRANSESOPHAGEAL ULTRASOUND TRANSDUCER (MTP7-4)
2
Total
2
Cleared
0
Denied
Atl Ultrasound, Inc. has 2 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 2 cleared submissions from 2000 to 2000. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Atl Ultrasound, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Atl Ultrasound, Inc.
2 devices