RM Electrode (RMH 23-01)
Dec 2023
129d
Retmap, Inc.
1
Total
1
Cleared
0
Denied
Retmap, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Dec 2023. Active since 2023. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Retmap, Inc. Filter by specialty or product code using the sidebar.
1 devices