# K922445: Vacu-Pro

- Pathway: 510(k) (Traditional)
- Applicant: Concord/Portex
- Decided: Aug 12, 1992 after 82 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.
14 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K081229: Saf-T Closed Blood Collection System with Saf-Holder Device, with 21G, 23G, 25G Saf-T Wing (2008), 13 descendants of its own
- K142946: TIVA (2015), 8 descendants of its own
- K152924: TIVA¿ (2016), 7 descendants of its own
- K163508: PIVO (2017), 6 descendants of its own
- K190604: PIVO (2019), 5 descendants of its own

Source page: https://510kreport.com/device/K922445
Methodology: https://510kreport.com/methodology