# K921520: Vacutainer Brand Luer Adapter

- Pathway: 510(k) (Traditional)
- Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Decided: Jul 10, 1992 after 101 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
No predicates in its family tree.
3 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K980768: Vacuette Holdex (1998), 2 descendants of its own
- K160532: Greiner Holdex (2016), 1 descendant of its own
- K180545: VACUETTE SAFELINK Holder with male luer lock (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K921520
Methodology: https://510kreport.com/methodology