# K192035: EvaQMax Smoke Evacuation System

- Pathway: 510(k) (Traditional)
- Applicant: Bio Protech, Inc.
- Decided: Aug 29, 2019 after 30 days
- Product code: FYD (Apparatus, Exhaust, Surgical)
- Device class: 2
- Regulation: 21 CFR 878.5070
- 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’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
To remove and filter smoke and aerosols from a surgical site produced during electrosurgical and laser procedures.

Source page: https://510kreport.com/device/K192035
Methodology: https://510kreport.com/methodology