# K893987: Nidek Model YC-1200

- Pathway: 510(k) (Traditional)
- Applicant: Nidek, Inc.
- Decided: Aug 18, 1989 after 74 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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 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
- K973470: Coherent Popeye Ophthalmic Laser System, Coherent Popeye Ophthalmic Laser System in Combination with the Coherent Argons (1997), 8 descendants of its own
- K032357: Novus TTX Laser and Delivery Devices with Accessories (2003), 5 descendants of its own
- K052526: Novus 3000 Laser System and Delivery Devices (2005), 4 descendants of its own
- K062336: Optimedica Laser Indirect Ophthalmoscope (2006), 1 descendant of its own
- K061025: Accutech Endolite Probe (2006), 1 descendant of its own

## Recalls of this device
- Mar 6, 2015 · Class II · Z-1367-2015: Dear Doctor letter and Quick Reference Guide is being sent to users of the YC-1800 to reiterate important safety and cleaning information after complaints of pitting lens that may cause unclear images

Source page: https://510kreport.com/device/K893987
Methodology: https://510kreport.com/methodology