PMA supplement
P940034 S002: GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
FDA PMA supplement · Special (Immediate Track) · Gen-Probe, Inc.
Key facts
| Original PMA | P940034 |
|---|---|
| Supplement number | S002 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST) |
| Generic name | System, nucleic acid amplification, mycobacterium tuberculosis complex |
| Applicant | Gen-Probe, Inc. |
| Product code | MWA |
| Received date | May 22, 1996 |
| Decision date | Jun 5, 1996 |
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: