# K943489: Disposable Surgical Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Resources
- Decided: Aug 9, 1994 after 21 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K072674: Kii Trocar System (2007), 2 descendants of its own
- K231400: Bladeless Trocar – Artemis Lap Cannula (2023), 0 descendants of its own
- K111002: Reprocessed Endoscopic Trocars (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K943489
Methodology: https://510kreport.com/methodology