# K931784: HGM Illuminating Imaging Endocular Probe

- Pathway: 510(k) (Traditional)
- Applicant: Hgm, Inc.
- Decided: Mar 1, 1994 after 326 days
- Product code: HQF (Laser, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.4390
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 4 cite it directly.
0 of 16 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
- 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
- K052526: Novus 3000 Laser System and Delivery Devices (2005), 4 descendants of its own
- K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator (2015), 2 descendants of its own
- K062336: Optimedica Laser Indirect Ophthalmoscope (2006), 1 descendant of its own

Source page: https://510kreport.com/device/K931784
Methodology: https://510kreport.com/methodology