# K982309: Smoke Evacuation Attachment 130XXX TBD

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: Aug 5, 1998 after 35 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 devices 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.

## Most influential descendants
- K081634: Conmed Goldvac Integrated Smoke Evacuation Pencil (2008), 9 descendants of its own
- K120454: Safeair Smoke Pencil, (2012), 8 descendants of its own
- K142538: LiNA SafeAir Smoke Pencil (2014), 5 descendants of its own
- K143145: SafeAir Smoke Pencil (2014), 4 descendants of its own
- K153679: Stryker Neptune E-SEP Smoke Evacuation Pencil (2016), 3 descendants of its own

## Indications for use
Used in conjunction with the electrosurgical pencil of 510(k) Notification K791137, the accessory is intended to remove smoke generated by electrosurgery.

Source page: https://510kreport.com/device/K982309
Methodology: https://510kreport.com/methodology