# K940393: Peregrine Wide Angle Light Pipe

- Pathway: 510(k) (Traditional)
- Applicant: Peregrine Surgical, Ltd.
- Decided: Sep 2, 1994 after 219 days
- Product code: HJM (Transilluminator, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1945
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K972506: Infinitech Bullet Endo Illuminated Pick Manipulator (1997), 0 descendants of its own

## Recalls of this device
- Nov 10, 2003 · Not classified · Z-0264-04: The CX9625 Light Pipe connector may overheat; this condition could result in the plastic connector that plugs into the Millennium Microsurgical System to malfunction.

Source page: https://510kreport.com/device/K940393
Methodology: https://510kreport.com/methodology