# K022130: BD Vacutainer Plus PST II Tube

- Pathway: 510(k) (Traditional)
- Applicant: Becton, Dickinson & CO
- Decided: Jul 29, 2002 after 28 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: 1 generation back to K945952 (1995). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K945952: Vacutainer (R) Brand Plus PST (TM) Plasma Separation Tube, Bd Becton Dickinson Vacutainer Systems Preanalytic (1995) Summary page 3.

## Most influential descendants
- K161521: TAP Blood Collection Device (2017), 1 descendant of its own
- K190225: TAP Blood Collection Device (2019), 0 descendants of its own

## Indications for use
The BD Vacutainer PLUS PST II Tube is a lithium heparin coated plastic evacuated blood collection tube that provides a means of collecting, transporting and processing blood in a closed tube. Blood collected in a Vacutainer PLUS PST II Tube is used for clinical laboratory assays involving the use of patient plasma.

Source page: https://510kreport.com/device/K022130
Methodology: https://510kreport.com/methodology