PMA supplement
P900025 S001: FLUORO-CEP (R) PROGESTERONE
FDA PMA supplement · Normal 180 Day Track · Zeus Scientific, Inc.
Key facts
| Original PMA | P900025 |
|---|---|
| Supplement number | S001 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | FLUORO-CEP (R) PROGESTERONE |
| Generic name | KIT, ASSAY, PROGESTERONE RECEPTOR |
| Applicant | Zeus Scientific, Inc. |
| Product code | LPI |
| Received date | Dec 11, 1991 |
| Decision date | Apr 21, 1992 |
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: