# K944607: Model 5135 Auto LP/Flash

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Dec 13, 1994 after 85 days
- Product code: GCT (Light Source, Endoscope, Xenon Arc)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K981804: Xenon Light Source Model LS6000 (1998), 1 descendant of its own
- K982962: Xenon Light Source, Models LS6180, LS6035 (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K944607
Methodology: https://510kreport.com/methodology