Sensititre , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sensititre , Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Sensititre , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Salem, US.
Historical record: 3 cleared submissions from 1988 to 1996. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Sensititre , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sensititre , Ltd.
3 devices