# K042487: Procedur SF Safety Syringe Device

- Pathway: 510(k) (Traditional)
- Applicant: Avanca Medical Devices, Inc.
- Decided: Jan 21, 2005 after 130 days
- Product code: MEG (Syringe, Antistick)
- Device class: 2
- Regulation: 21 CFR 880.5860
- 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 K980069 (1998). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980987: Becton Dickinson Syringe, Bd Becton Dickinson Vacutainer Systems Preanalytic (1998) Summary page 1.
- K980069: Vanishpoint Syringe, Retractable Technologies, Inc. (1998) Summary page 1.

## Indications for use
The Procedur-SF device is used to inject fluids into, or withdraw fluids from, the body, while reducing the risk of sharps injuries and the potential for syringe reuse.

Source page: https://510kreport.com/device/K042487
Methodology: https://510kreport.com/methodology