# K952213: Alcon Series 20000 Legacy Phacoemulsifier

- Pathway: 510(k) (Traditional)
- Applicant: Alcon Laboratories
- Decided: Aug 9, 1995 after 90 days
- Product code: HQC (Unit, Phacofragmentation)
- Device class: 2
- Regulation: 21 CFR 886.4670
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
77 later devices descend from it; 6 cite it directly.
0 of 78 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
- K993154: Laser Photolysis System, Pharo Ophthalmic Surgery System (2000), 49 descendants of its own
- K094052: Lensx 550 Laser System. Model 550 (2010), 47 descendants of its own
- K101626: Lensx Laser System (2010), 30 descendants of its own
- K063331: Bausch & Lomb NGX Microsurgical System (2006), 24 descendants of its own
- K082473: Bausch & Lomb Stellaris Microsurgical System (2009), 22 descendants of its own

Source page: https://510kreport.com/device/K952213
Methodology: https://510kreport.com/methodology