Precision GI
Aug 2023
103d
Limaca Medical, Ltd.
1
Total
1
Cleared
0
Denied
Limaca Medical, Ltd. — FDA 510(k) Submissions
Limaca Medical, Ltd. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Biopsy Needle . Use the specialty filter in the sidebar to narrow results.
1 devices