Meditech Endoscopy, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Meditech Endoscopy, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Scope ProTech
1
Total
1
Cleared
0
Denied
Meditech Endoscopy, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Basildon, GB.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Meditech Endoscopy, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accelerated Device Approval Services as regulatory consultant.
FDA 510(k) Regulatory Record - Meditech Endoscopy, Ltd.
1 devices