PMA supplement
P980018 S021: DAKO HERCEPTEST
FDA PMA supplement · Real-Time Process · Agilent Technologies Singapore (International) Pte, Ltd.
Key facts
| Original PMA | P980018 |
|---|---|
| Supplement number | S021 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | DAKO HERCEPTEST |
| Generic name | SYSTEM, TEST, HER-2/NEU, IHC |
| Applicant | Agilent Technologies Singapore (International) Pte , Ltd. |
| Product code | MVC |
| Received date | Feb 29, 2016 |
| Decision date | May 27, 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: