Swr International, Ltd. is one of 18354 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Swr International, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AXS-590 SERIES
1
Total
1
Cleared
0
Denied
Swr International, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Newington, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Swr International, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Swr International, Ltd.
1 devices