Fujifilm Medwork GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Fujifilm Medwork GmbH has 2 FDA 510(k) cleared medical devices. Based in Hochstadt, DE.
Last cleared in 2022. Active since 2021. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Fujifilm Medwork GmbH Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Fujifilm Medical Systems U.S.A, Inc. and FUJIFILM Healthcare Americas Corporation.
2 devices