PMA supplement
P200013 S011: Alinity m HBV
FDA PMA supplement · Special (Immediate Track) · Abbott Molecular, Inc.
Key facts
| Original PMA | P200013 |
|---|---|
| Supplement number | S011 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | Alinity m HBV |
| Generic name | Hepatitis Viral B DNA Detection |
| Applicant | Abbott Molecular, Inc. |
| Product code | MKT |
| Received date | Dec 7, 2022 |
| Decision date | Dec 22, 2022 |
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: