# K854929: Oxoid Streptococal Grouping Kit

- Pathway: 510(k) (Traditional)
- Applicant: Oxoid U.S.A., Inc.
- Decided: Mar 11, 1986 after 91 days
- Product code: GTZ (Antisera, All Groups, Streptococcus Spp.)
- Device class: 1
- Regulation: 21 CFR 866.3740
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K962296: Streptolex-Stat (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K854929
Methodology: https://510kreport.com/methodology