PMA supplement
P180048 S015: LIAISON XL MUREX HBeAg and LIAISON XL MUREX Control HBeAg
FDA PMA supplement · 30-Day Notice · DiaSorin, Inc.
Key facts
| Original PMA | P180048 |
|---|---|
| Supplement number | S015 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | LIAISON XL MUREX HBeAg and LIAISON XL MUREX Control HBeAg |
| Generic name | Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen) |
| Applicant | DiaSorin, Inc. |
| Product code | LOM |
| Received date | May 9, 2024 |
| Decision date | Jun 4, 2024 |
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: