# K131842: Sterican Cannula

- Pathway: 510(k) (Traditional)
- Applicant: B.Braun Medical, Inc.
- Decided: Aug 20, 2013 after 60 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K944931 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K944931: Becton Dickinson Blunt Steel Cannula, Bd Becton Dickinson Vacutainer Systems Preanalytic (1995) Summary page 1.

## Indications for use
The Sterican™ Cannula is intended for the aspiration of fluids for fluid transfer and may be used with a syringe for transferring fluids from stoppered vials, glass or plastic ampoules. The Sterican™ Cannula is intended for drug admixture only.

Source page: https://510kreport.com/device/K131842
Methodology: https://510kreport.com/methodology