PMA supplement
P820060 S003: ABBOTT AFP-EIA DIAGNOSTIC KIT FOR CANCER
FDA PMA supplement · Abbott Laboratories
Key facts
| Original PMA | P820060 |
|---|---|
| Supplement number | S003 |
| Trade name | ABBOTT AFP-EIA DIAGNOSTIC KIT FOR CANCER |
| Generic name | KIT, TEST,ALPHA-FETOPROTEIN FOR TESTICULAR CANCER |
| Applicant | Abbott Laboratories |
| Product code | LOJ |
| Received date | May 15, 1986 |
| Decision date | Mar 9, 1987 |
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: