# K911462: Surgical Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical
- Decided: Apr 22, 1991 after 19 days
- Product code: DRC (Trocar)
- Device class: 2
- Regulation: 21 CFR 870.1390
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K133375: Banyan Medical Disposable Secondary Cannula and Trocar (2014), 0 descendants of its own

## Recalls of this device
- Mar 12, 2018 · Class II · Z-1584-2018: Products have been packaged with the wrong Trocar length type.
- Sep 13, 2013 · Class II · Z-0147-2015: CooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shipper.

Source page: https://510kreport.com/device/K911462
Methodology: https://510kreport.com/methodology