# K872136: 12.5MM Peyman Wide Field Yag Laser Lens

- Pathway: 510(k) (Traditional)
- Applicant: Ocular Instruments, Inc.
- Decided: Jun 19, 1987 after 16 days
- Product code: HJK (Lens, Contact, Polymethylmethacrylate, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 886.1385
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K201909: RxSight Contact Lens (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K872136
Methodology: https://510kreport.com/methodology