# K042486: Procedur 10 Syringe Device

- Pathway: 510(k) (Traditional)
- Applicant: Avanca Medical Devices, Inc.
- Decided: Jan 21, 2005 after 130 days
- Product code: FMF (Syringe, Piston)
- 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 K980987 (1998). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
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.

## Most influential descendants
- K052075: Procedur-10 (2005), 0 descendants of its own

## Indications for use
The Procedur-10 device is used to inject fluids into, or withdraw fluids from, the body.

Source page: https://510kreport.com/device/K042486
Methodology: https://510kreport.com/methodology