# K233653: Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga  (3269.M04-00)

- Pathway: 510(k) (Traditional)
- Applicant: Peregrine Surgical, LLC
- Decided: Aug 5, 2024 after 265 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: 5 generations back to K954307 (1995). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator, Peregrine Surgical, Ltd. (2015) Summary page 7.

## Indications for use
The Midfield Light Pipe is a disposable microsurgical instrument used to conduct a field of light to the posterior segment of the eye in order to visualize the internal structures of the eyes during ophthalmic surgery.

Source page: https://510kreport.com/device/K233653
Methodology: https://510kreport.com/methodology