PMA
P970055: BIOTRIN PARVOVIRUS IGM EIA (V619IMUS)
FDA PMA · ASSAY,ENZYME LINKED IMMUNOSORBENT,PARVOVIRUS B19 IGM · Diasorin
Key facts
| PMA number | P970055 |
|---|---|
| Trade name | BIOTRIN PARVOVIRUS IGM EIA (V619IMUS) |
| Generic name | ASSAY,ENZYME LINKED IMMUNOSORBENT,PARVOVIRUS B19 IGM |
| Applicant | Diasorin |
| Owner/operator | DiaSorin Inc. |
| Product code | MYM |
| Approval date | Aug 6, 1999 |
| Docket number | 00M-1215 |
| Establishment registration | 2182595 |
| FEI number | 2182595 |
At a glance
- 10–99 Supplements
- Jan 6, 2025 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- None UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: