Fujifilm Irvine Scientific

Fujifilm Irvine Scientific — FDA 510(k) Submissions

Fujifilm Irvine Scientific has submitted 4 FDA 510(k) premarket notifications since 2023, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Reproductive, Media, Culture, Ex Vivo, Tissue And Cell, Labware, Assisted Reproduction . Use the specialty filter in the sidebar to narrow results.