# K992508: TSX Probe, Ocular Contact Probe;TSX Probe,Ocular Contact Probe,Sma

- Pathway: 510(k) (Traditional)
- Applicant: Instruments For Medicine and Diagnostics
- Decided: Aug 19, 1999 after 23 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Iris G-Probe: named in the summary without a submission number

## Indications for use
Contact Transscleral Cyclophotocoagulation (CYC) for the reduction of intra ocular pressure (IOP) in glaucoma patients. This ocular contact probe to be used with approved infrared laser devices for this procedure. Ablation of the Ciliary Body in glaucoma patients.

Source page: https://510kreport.com/device/K992508
Methodology: https://510kreport.com/methodology