Direct Access Diagnostics
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K964108 | FACT PLUS PREGNANCY TEST | LCX | 1996-11-18 | View |
| 510(k) | K962521 | FACTPLUS ONE STEP PREGNANCY TEST | LCX | 1996-07-29 | View |
No matching devices.
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