A Mano Products, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
A Mano Products, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
A Mano Products, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by A Mano Products, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A Mano Products, Ltd.
1 devices