K243725
- 510(k) number
- K243725
- Device name
- BD Vaginal Panel
- Applicant
- Becton, Dickinson and Company MD · US
- Product code
- PQA — Vaginitis And Bacterial Vaginosis Nucleic Acid Detec
- Decision date
- 2024-12-19
- Date received
- 2024-12-03
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Microbiology
510(k) Summary (official FDA PDF): K243725.pdf
Official FDA record: K243725
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.