# K131040: Extavipro Sterican 30G

- Pathway: 510(k) (Traditional)
- Applicant: B.Braun Melsungen AG
- Decided: Jul 15, 2013 after 91 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: 3 generations back to K931367 (1993). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072247: Sterican Hypodermic Needles, B.Braun Medical, Inc. (2007) Summary page 2.

## Indications for use
ExtaviPro™ Sterican™ 30G Hypodermic needles, when attached to a male connector, are intended to be used to inject fluid into, or withdraw fluids from, parts of the body below the surface of the skin.

Source page: https://510kreport.com/device/K131040
Methodology: https://510kreport.com/methodology