DENSICOMP 250
Jan 1991
107d
L. Keroack Co.
1
Total
1
Cleared
0
Denied
L. Keroack Co. has 1 FDA 510(k) cleared medical devices. Based in Canada H3x 3p3, CA.
Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by L. Keroack Co. Filter by specialty or product code using the sidebar.
1 devices