# K954307: Gamp & Assoc. Disposable Endoocular Laser Probe

- Pathway: 510(k) (Traditional)
- Applicant: Gamp & Assoc.
- Decided: Dec 22, 1995 after 98 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
No predicates in its family tree.
16 later devices descend from it; 3 cite it directly.
0 of 17 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
- K024061: Peregrine Straight Laser Probe, Model PD6000.00 (2003), 11 descendants of its own
- 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
- K113857: Synergetics Directional Endoocular Laser Probe (2012), 3 descendants of its own
- K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator (2015), 2 descendants of its own

Source page: https://510kreport.com/device/K954307
Methodology: https://510kreport.com/methodology