# K022875: Modification to BD Vacutainer Push Button Blood Collection Set

- Pathway: 510(k) (Special)
- Applicant: Becton, Dickinson & CO
- Decided: Sep 11, 2002 after 12 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: 3 generations back to K970259 (1997). 6 ancestors in all.
18 later devices descend from it; 1 cites it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011984: BD Vacutainer Push Button Blood Colection Set, Becton, Dickinson & CO (2001)

## Most influential descendants
- K030573: BD Vacutainer Push Button Blood Collection Set, Models 367338, 367344, 367336, 367342, 367335, 367341 (2003), 17 descendants of its own
- K153309: BD Vacutainer UltraTouch Push Button Blood Collection Set (2016), 6 descendants of its own
- K192247: Steripath Gen2 Blood Collection System (2020), 5 descendants of its own
- K213718: SOL-GUARD Safety Pull Button Collection Set (2022), 2 descendants of its own
- K200661: Steripath Micro Blood Collection System (2020), 2 descendants of its own

## Indications for use
The BD Vacutainer™ Push Button Blood Collection Set is a sterile, multiple-sample, single-use winged blood collection set intended for venipuncture to obtain blood specimens from patients. The recommended use of the device is to activate the needle prior to removal from the venipuncture site. The retraction of the intravenous (IV) end of the needle aids in the prevention of needlestick injury.

Source page: https://510kreport.com/device/K022875
Methodology: https://510kreport.com/methodology