# K931072: HGM Illuminating/Aspirating Endoocular Probe

- Pathway: 510(k) (Traditional)
- Applicant: Hgm, Inc.
- Decided: Nov 10, 1994 after 618 days
- Product code: HJM (Transilluminator, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1945
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 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
- K052526: Novus 3000 Laser System and Delivery Devices (2005), 4 descendants of its own
- K062336: Optimedica Laser Indirect Ophthalmoscope (2006), 1 descendant of its own
- K061025: Accutech Endolite Probe (2006), 1 descendant of its own
- K123056: Pascal Laser Indirect Ophthalmoscope (2012), 0 descendants of its own
- K090281: Accutech Family of Powerflex Laser Delivery Devices (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K931072
Methodology: https://510kreport.com/methodology