PMA supplement
P800025 S004: QUANTITOPE 125I AFP KIT AND CONTROL SERUM
FDA PMA supplement · Bio-Rad Laboratories, Inc.
Key facts
| Original PMA | P800025 |
|---|---|
| Supplement number | S004 |
| Trade name | QUANTITOPE 125I AFP KIT AND CONTROL SERUM |
| Generic name | KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS |
| Applicant | Bio-Rad Laboratories, Inc. |
| Product code | LOK |
| Received date | Mar 18, 1986 |
| Decision date | Apr 21, 1988 |
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: