Pb Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K925703 | OPUS SEROLOGY CONTROLS | MJX | 1993-04-08 | View |
| 510(k) | K921523 | OPUS(R) TOXO-G TEST SYSTEM | LGD | 1992-09-14 | View |
| 510(k) | K915870 | OPUS RUBELLA TEST SYSTEM | LFX | 1992-03-23 | View |
| 510(k) | K913080 | OPUS(R) ANTI CMV-M | LKQ | 1991-10-28 | View |
No matching devices.
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