# K953918: Magnetic Resonance Diagnostic Device

- Pathway: 510(k) (Traditional)
- Applicant: Hitachi Medical Systems America, Inc.
- Decided: Sep 12, 1995 after 25 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- 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
- K982761: Joint Motion Device Package PN 1032,Kneel Cervical PN 1026, Lumbar 1027, Wrist 1028, Ankle 1029, Shoulder 1030, Hip 1031 (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K953918
Methodology: https://510kreport.com/methodology