# K946135: Infinitech Aspirating Laser Probe

- Pathway: 510(k) (Traditional)
- Applicant: Surgical Technologies, Inc.
- Decided: Apr 18, 1995 after 123 days
- Product code: HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 3 cite it directly.
0 of 11 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
- K050807: 20G Sma Laser Fiber, Model LF100 (2005), 6 descendants of its own
- K121187: Katalyst Laser Probes, Katalyst Illuminated Laser Probes (2012), 5 descendants of its own
- K142830: Ophthalmed Bending Laser Probes (2015), 2 descendants of its own
- K191846: MAXReach Laser Probe (2019), 1 descendant of its own
- K022228: Family of Iris Medical Endoprobe Handpieces (2002), 1 descendant of its own

Source page: https://510kreport.com/device/K946135
Methodology: https://510kreport.com/methodology