PMA supplement
P050045 S003: TOP2A FISH PHARMDX KIT
FDA PMA supplement · 30-Day Notice · Dako Denmark A/S
Key facts
| Original PMA | P050045 |
|---|---|
| Supplement number | S003 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | TOP2A FISH PHARMDX KIT |
| Generic name | Fluorescence in situ hybridization, topoisomerase ii alpha, gene amplification and deletion |
| Applicant | Dako Denmark A/S |
| Product code | NXG |
| Received date | Oct 6, 2011 |
| Decision date | Nov 10, 2011 |
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: