Inmark Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Inmark Corp. has 4 FDA 510(k) cleared medical devices. Based in Norwalk, US.
Historical record: 4 cleared submissions from 1989 to 1991. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Inmark Corp. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Mar 27, 1991
X-RAY TUBE HOUSING ASSEMBLY POLARIX II GEN/XO 110
Radiology
62d
Cleared
Mar 06, 1991
X-RAY TUBE HOUSING ASSEMBLY SOREDEX DC/CIR 51
Radiology
42d
Cleared
Oct 27, 1989
RELOADING OF X-RAY TUBE HOUSING ASSEM., VARIOUS
Radiology
102d
Cleared
Sep 22, 1989
X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS
Radiology
67d