# K961158: Suprasson P5 Booster

- Pathway: 510(k) (Traditional)
- Applicant: Satelec
- Decided: May 23, 1996 after 62 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
Longest line of descent: 1 generation back to K942139 (1995). 1 ancestor in all.
26 later devices descend from it; 6 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)
- K942139: Suprasson P Max, Satelec (1995) Summary page 1.

## Most influential descendants
- 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
- K102218: Compact Piezo P2K, Powercare (2011), 3 descendants of its own

## Indications for use
The SUPRASSON P-Max and SUPRASSON P5 are intended to provide overall prophylaxis and preservation of soft and hard tissue during the 3 standard dental treatments; Scaling, Periodontics, and Endodontics.

Source page: https://510kreport.com/device/K961158
Methodology: https://510kreport.com/methodology