# P840047: Cilco ND:Yag Laser

- Pathway: PMA
- Applicant: Coopervision-Cilco
- Decided: Aug 2, 1985 after 304 days
- Product code: LXS (Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla)
- Device class: 2
- Regulation: 21 CFR 886.4392
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P840047
Methodology: https://510kreport.com/methodology