# K000158: Veinlase, Model E50-K8-B5, Spectrum K8, Model E50-K8-B9

- Pathway: 510(k) (Traditional)
- Applicant: Fisma, Inc.
- Decided: Aug 24, 2000 after 218 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. FDA has not posted a summary or statement for it, so its predicates are not known.

Source page: https://510kreport.com/device/K000158
Methodology: https://510kreport.com/methodology