Oxyless, Ltd. is one of 367 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Oxyless, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Oxyless Blood Tubing Set
1
Total
1
Cleared
0
Denied
Oxyless, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Oxyless, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bob Duffy Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Oxyless, Ltd.
1 devices