# K920110: Endopath Disposable Thoracic Trocar Sleeve

- Pathway: 510(k) (Traditional)
- Applicant: ETHICON, Inc.
- Decided: Apr 2, 1992 after 86 days
- Product code: GEA (Cannula, Surgical, General & Plastic Surgery)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
17 later devices descend from it; 1 cites it directly.
0 of 18 devices 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.

## Most influential descendants
- K112358: Unimax Trocar System (2011), 16 descendants of its own
- K133845: 8MM Trocar Kit (2014), 6 descendants of its own
- K141594: Unimicro Trocar Kit, models: Auto-Locking Trocar, Hasson Trocar, Bladeless Trocar (2015), 5 descendants of its own
- K181395: Universal Cannula Seal (5-12 mm) (2018), 4 descendants of its own
- K231358: Universal Seal (5-12 mm) (2023), 3 descendants of its own

Source page: https://510kreport.com/device/K920110
Methodology: https://510kreport.com/methodology