Alerchek, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K885307 | FLIPSCREEN (TM) TOTAL E IMMUNOASSAY | DGC | 1989-03-08 | View |
| 510(k) | K874802 | FLIPSCREEN QAT | DHB | 1988-02-17 | View |
| 510(k) | K860027 | FLIPSCREEN SPECIFIC E (PE, SE, NE, SW, NW) ASSAY | DHB | 1986-04-22 | View |
No matching devices.
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