# K932995: Surgical Trocar and Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Resources
- Decided: Sep 23, 1993 after 97 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.
14 later devices descend from it; 3 cite it directly.
0 of 15 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
- K060096: Modular Trocar System (2006), 10 descendants of its own
- K083638: Fixation Trocars (2008), 4 descendants of its own
- K211577: SoftFix Balloon Trocar (2021), 2 descendants of its own
- K072674: Kii Trocar System (2007), 2 descendants of its own
- K012968: Applied Access Seal (2001), 2 descendants of its own

Source page: https://510kreport.com/device/K932995
Methodology: https://510kreport.com/methodology