# K003638: Mojave Cataract Extraction System

- Pathway: 510(k) (Abbreviated)
- Applicant: Allergan, Inc.
- Decided: Feb 13, 2001 after 81 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.
33 later devices descend from it; 2 cite it directly.
0 of 34 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
- K060366: The Amo Ophthalmic Surgical System (2006), 32 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
- K101325: Stellaris PC Vision Enhancement System (2010), 14 descendants of its own
- K081877: Associate 2500 Dual and Compact Systems (2009), 8 descendants of its own

Source page: https://510kreport.com/device/K003638
Methodology: https://510kreport.com/methodology