# K000832: Sterotactic Localization Device (SLD)

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems North America, Inc.
- Decided: Apr 27, 2000 after 44 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K020289: Mics Intervention Aid, Catalog # Mics-Mia and Mics-Mias (2002), 3 descendants of its own
- K090223: Icad Breast Interventional Planning Software, Model D70024 (2009), 0 descendants of its own
- K071534: Confirma Breast Mri Interventional Components (2007), 0 descendants of its own
- K041020: Cadstream Version 3.1 (2004), 0 descendants of its own
- K023686: Aurora MR-Guided Interventional System (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K000832
Methodology: https://510kreport.com/methodology