# K950721: Fuji Medical Laser Imagermulti-Formatters MF-300 and MF-300L

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: May 24, 1995 after 97 days
- Product code: LMC (Camera, Multi Format, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K970349: Fuji Medical Laser Imager MF Print Server MF-PS667 (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K950721
Methodology: https://510kreport.com/methodology