Alexon, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
Advertisement
Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K934493 | PROSPECT MICROPLATE ASSAY | LLH | 1994-09-20 | View |
| 510(k) | K942098 | PROSPECT GIARDIA | MHI | 1994-09-09 | View |
| 510(k) | K931147 | PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATION | MHI | 1993-05-13 | View |
| 510(k) | K930451 | PROSPEC T GIARDIA MICROTITER ASSAY | MHI | 1993-04-21 | View |
| 510(k) | K922675 | PROSPECT GIARDIA CONTROLS | MHI | 1992-09-11 | View |
| 510(k) | K922010 | PROSPECT(TM) GIARDIA MICROTITER ASSAY/MODIFICATION | MHI | 1992-06-19 | View |
| 510(k) | K920817 | MODIFICATION PROSPECT GIARDIA RAPID ASSAY | MHI | 1992-04-22 | View |
| 510(k) | K912242 | PROSPECT(TM/CRYPTOSPORIDIUM | MHJ | 1992-03-23 | View |
| 510(k) | K915093 | PROSPECT(TM) GIARDIA RAPID ASSAY | MHI | 1992-01-30 | View |
| 510(k) | K911337 | PROSPEC T/GIARDIA RAPID ASSAY | MHI | 1991-09-27 | View |
No matching devices.
Advertisement