Nipro Company, Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Nipro Company, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Nipro Company, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Osaka, JP.
Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Nipro Company, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nipro Company, Ltd.
1 devices