Instrumentarium Corp. Imaging Division is one of 23598 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Instrumentarium Corp. Imaging Division - FDA 510(k) Cleared Devices
Recent clearances: ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D, PERFORMA STEREO, DELTA 32
3
Total
3
Cleared
0
Denied
Instrumentarium Corp. Imaging Division has 3 FDA 510(k) cleared medical devices. Based in Milwaukee, US.
Historical record: 3 cleared submissions from 2002 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Instrumentarium Corp. Imaging Division Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Instrumentarium Corp. Imaging Division
3 devices