PMA supplement
P160037 S021: Onclarity HPV Assay
FDA PMA supplement · Normal 180 Day Track No User Fee · Becton, Dickinson and Company
Key facts
| Original PMA | P160037 |
|---|---|
| Supplement number | S021 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Postapproval Study Protocol |
| Trade name | Onclarity HPV Assay |
| Generic name | KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS |
| Applicant | Becton, Dickinson and Company |
| Product code | MAQ |
| Received date | Feb 11, 2025 |
| Decision date | Mar 12, 2025 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: