# K942139: Suprasson P Max

- Pathway: 510(k) (Traditional)
- Applicant: Satelec
- Decided: Sep 29, 1995 after 514 days
- Product code: ELC (Scaler, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 872.4850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
27 later devices descend from it; 2 cite it directly.
0 of 28 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
- K961158: Suprasson P5 Booster (1996), 26 descendants of its own
- K972026: SP4044 & SP4055 Lux Modules (1997), 21 descendants of its own
- K033764: SP Newtron Module (2004), 20 descendants of its own
- K050895: Surpasson P5 Newtron (2005), 11 descendants of its own
- K202906: EndoPilot2 (2021), 4 descendants of its own

Source page: https://510kreport.com/device/K942139
Methodology: https://510kreport.com/methodology