# K963953: Imig-Mri

- Pathway: 510(k) (Traditional)
- Applicant: Imig-Mri Systems, LLC
- Decided: Dec 18, 1996 after 77 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Siemens Magnetom P8: named in the summary without a submission number

## Most influential descendants
- K983902: Field Effects Mri System (1999), 0 descendants of its own
- K982157: Trex Mri Magnetic Resonance Diagnostic Device (1998), 0 descendants of its own

## Indications for use
Anatomy: head, limbs, spine, torso; Nuclei: H-1; Diagnostic uses: Imaging

Source page: https://510kreport.com/device/K963953
Methodology: https://510kreport.com/methodology