# K132614: Peregrine Curved Illuminating Laser Probe

- Pathway: 510(k) (Special)
- Applicant: Peregrine Surgical, Ltd.
- Decided: Nov 14, 2013 after 85 days
- Product code: HQB (Photocoagulator And Accessories)
- Device class: 2
- Regulation: 21 CFR 886.4690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K954307 (1995). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031023: Peregrine Illuminating Laser Probe Model PD600.10, Peregrine Surgical, Ltd. (2003) Summary page 2.

## Indications for use
For photocoagulation and illumination during ophthalmic surgery. This device delivers illumination as well as 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/K132614
Methodology: https://510kreport.com/methodology