# P860042: Trimedyne's Laserprobe-PLR{TM} Catheter & Optilase

- Pathway: PMA
- Applicant: Trimedyne, Inc.
- Decided: Feb 27, 1987 after 178 days
- Product code: LWX (Device. Laser Peripheral Angioplasty)
- Device class: 3
- 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. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P860042
Methodology: https://510kreport.com/methodology