# K022426: BD Preset Blood Collection Syringe, BD a-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538

- Pathway: 510(k) (Special)
- Applicant: Becton, Dickinson & CO
- Decided: Aug 8, 2002 after 14 days
- Product code: JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection)
- Device class: 2
- Regulation: 21 CFR 862.1675
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K875117 (1988). 3 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982922: Vacutainer Brand Blood Collection Syringe, Becton Dickinson Vacutainer Systems (1998) Summary page 3.

## Most influential descendants
- K260128: BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes (2026), 0 descendants of its own
- K202446: BD Preset Syringe & BD A-Line Syringe (2020), 0 descendants of its own

## Indications for use
BD PresetTMand BD A-LineTMBlood Collection Syringe are intended to collect whole blood specimens for diagnostic testing which may include: pH, blood gases, electrolytes (including ionized calcium), metabolytes, co-oximetry, and other tests

Source page: https://510kreport.com/device/K022426
Methodology: https://510kreport.com/methodology