Oxyless, Ltd. is one of 167 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Oxyless, Ltd. - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Oxyless, Ltd.
1 devices