Novaprobe Incorporated is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novaprobe Incorporated - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Novaprobe Incorporated has 1 FDA 510(k) cleared medical devices. Based in Lansdale, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Novaprobe Incorporated Filter by specialty or product code using the sidebar.
Novaprobe Incorporated — FDA 510(k) Products and Clearance History
1 devices