# K024061: Peregrine Straight Laser Probe, Model PD6000.00

- Pathway: 510(k) (Traditional)
- Applicant: Peregrine Surgical, Ltd.
- Decided: Mar 7, 2003 after 88 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K954307 (1995). 2 ancestors in all.
11 later devices descend from it; 4 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954307: Gamp & Assoc. Disposable Endoocular Laser Probe, Gamp & Assoc. (1995) Summary page 2.
- K980797: Peregrine Fiber Optic Multi-Function Manipulator, Peregrine Surgical, Ltd. (1998) Summary page 2.

## Most influential descendants
- K031023: Peregrine Illuminating Laser Probe Model PD600.10 (2003), 6 descendants of its own
- K122997: 23GA Curved Illuminating Laser Probe (2013), 4 descendants of its own
- K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator (2015), 2 descendants of its own
- K213467: EVA NEXUS Ophthalmic Surgical System (2022), 1 descendant of its own
- K250501: System Sophi (2025), 0 descendants of its own

## Indications for use
For photocoagulation during ophthalmic surgery. This device delivers laser energy to target tissue, causing coagulation. Spot size can be varied by altering the distance between the tissue and the probe tip.

Source page: https://510kreport.com/device/K024061
Methodology: https://510kreport.com/methodology