# K930193: Philips Endo-Cavitary Mri Coil

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: Jun 24, 1994 after 526 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K981410: Hammersmith Endocavitary Coils (1998), 1 descendant of its own
- K011683: Nurvo 9000 Endocavitary Coils (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K930193
Methodology: https://510kreport.com/methodology