PMA supplement
BP120001 S305: OraQuick® In-Home HIV Test
FDA PMA supplement · 30-Day Notice · OraSure Technologies, Inc
Key facts
| Original PMA | BP120001 |
|---|---|
| Supplement number | S305 |
| Supplement type | 30-Day Notice |
| Trade name | OraQuick® In-Home HIV Test |
| Generic name | Hiv self-tests |
| Applicant | OraSure Technologies, Inc |
| Product code | QSS |
| Received date | Nov 28, 2016 |
| Decision date | Dec 23, 2016 |
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: