# K923133: Affirm/VP Ident.Test G.Vaginalis & T.Vaginalis

- Pathway: 510(k) (Traditional)
- Applicant: Microprobe Corp.
- Decided: Sep 25, 1992 after 88 days
- Product code: MJM (Dna Probe, Gardnerella Vaginalis)
- Device class: 1
- Regulation: 21 CFR 866.2660
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K993732: Bvblue (2000), 0 descendants of its own

Source page: https://510kreport.com/device/K923133
Methodology: https://510kreport.com/methodology