# K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator

- Pathway: 510(k) (Traditional)
- Applicant: Peregrine Surgical, Ltd.
- Decided: Sep 11, 2015 after 88 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: 4 generations back to K954307 (1995). 7 ancestors in all.
2 later devices descend from it; 2 cite 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)
- K980025: Peregrine Tapered Diffusion Probe, Peregrine Surgical, Ltd. (1998) Summary page 4.
- K122997: 23GA Curved Illuminating Laser Probe, Peregrine Surgical, Ltd. (2013) Summary page 4.

## Most influential descendants
- K233653: Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga  (3269.M04-00) (2024), 0 descendants of its own
- K182646: Vitreq disposable laser probes, light fibers and Chandelier (2019), 0 descendants of its own

## Indications for use
Adjustable Chandelier Illuminator family of ophthalmic illuminators is for wide angle illumination during ophthalmic surgery.

Source page: https://510kreport.com/device/K151604
Methodology: https://510kreport.com/methodology