# K202670: Nam illumination probe with chopper

- Pathway: 510(k) (Traditional)
- Applicant: Oculight, Ltd.
- Decided: Aug 20, 2021 after 340 days
- Product code: MPA (Endoilluminator)
- 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
Longest line of descent: 2 generations back to K875004 (1988). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K973290: Syntec True Light Endoillumiinator with Pick, Vaughan Weeks (1997) Summary page 4.

## Indications for use
The Nam illumination probe with chopper is used to illuminate with visible spectrum light the intraocular portion of the eye for improved visualization and manipulation during cataract surgery.

Source page: https://510kreport.com/device/K202670
Methodology: https://510kreport.com/methodology