# K925129: Selector

- Pathway: 510(k) (Traditional)
- Applicant: Spembly Medical, Ltd.
- Decided: Apr 23, 1993 after 192 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- 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.
18 later devices descend from it; 1 cites it directly.
0 of 19 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
- K042277: Selector Quantum Ultrasonic Aspirator System (2004), 17 descendants of its own
- K081459: Cusa Selector NXT Ultrasonic Tissue Ablation System (2008), 16 descendants of its own
- K161882: CUSA Clarity Ultrasonic Surgical Aspirator System (2016), 11 descendants of its own
- K182809: CUSA Clarity Ultrasonic Surgical Aspirator System (2018), 10 descendants of its own
- K200774: CUSA Clarity Ultrasonic Surgical Aspirator System (2020), 5 descendants of its own

Source page: https://510kreport.com/device/K925129
Methodology: https://510kreport.com/methodology