# SEP: Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

- Device class: 2; regulation: 21 CFR 866.2920; FDA's rule: 510(k) required
- FDA decisions: 2
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2025: 1
- 2026: 1

## Most-cited predicates
- DEN240045: Teal Wand (2025), cited by 2

Source page: https://510kreport.com/product-code/SEP
Data by year (CSV): https://510kreport.com/product-code/SEP.csv