# K000945: Para 12 Plus Retics

- Pathway: 510(k) (Traditional)
- Applicant: Streck Laboratories, Inc.
- Decided: Apr 18, 2000 after 26 days
- Product code: GLQ (Mixture, Control, White-Cell And Red-Cell Indices)
- Device class: 2
- Regulation: 21 CFR 864.8625
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K060083: NRBC-Chex for LH (2006), 1 descendant of its own
- K080016: NRBC-Chex for Advia (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K000945
Methodology: https://510kreport.com/methodology