Diamedix Corp.
FDA 510(k) & PMA Approved Devices — 68 products
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Total Devices68
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K093101 | MAGO 4S | LFX | 2011-01-21 | View |
| 510(k) | K021394 | DIAMEDIX IS-RHEUMATOID FACTOR TEST SYSTEM | DHR | 2002-07-09 | View |
| 510(k) | K013956 | DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I SCREEN | MSV | 2002-01-08 | View |
| 510(k) | K013628 | DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I IGG/IGM TEST SYSTEM | MSV | 2001-12-21 | View |
| 510(k) | K012449 | DIAMEDIX IS-ANTI-CARDIOLIPIN IGG/IGM TEST SYSTEM | MID | 2001-10-26 | View |
| 510(k) | K012450 | DIAMEDIX IS-ANTI-CARDIOLIPIN IGA TEST SYSTEM | MID | 2001-10-26 | View |
| 510(k) | K012797 | DIAMEDIX IS-ANTI-GLIADIN IGA TEST SYSTEM | MST | 2001-09-28 | View |
| 510(k) | K012795 | DIAMEDIX IS-ANTI-GLIADIN IGG TEST SYSTEM | MST | 2001-09-28 | View |
| 510(k) | K012053 | DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM | MID | 2001-08-20 | View |
| 510(k) | K002262 | DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM | LGC | 2000-11-28 | View |
| 510(k) | K001875 | DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM | LFX | 2000-08-21 | View |
| 510(k) | K001767 | DIAMEDIX IS-CMV IGM CAPTURE TEST SYSTEM | LJO | 2000-08-07 | View |
| 510(k) | K001707 | DIAMEDIX IS-TOXOPLASMA IGM CAPTURE TEST SYSTEM | LGD | 2000-07-07 | View |
| 510(k) | K994424 | DIAMEDIX IS-ANTI-DSDNA TEST SYSTEM | LRM | 2000-02-18 | View |
| 510(k) | K993294 | DIAMEDIX IS-ANA ELISA SCREEN TEST SYSTEM | LKJ | 1999-10-25 | View |
| 510(k) | K981812 | EBV-VCA IGG ELISA TEST SYSTEM | LSE | 1999-03-04 | View |
| 510(k) | K981829 | IS EBV-EBNA-1 IGG ELISA TEST SYSTEM | GNP | 1999-02-16 | View |
| 510(k) | K981831 | IS EBV-EA-D IGG ELISA TEST SYSTEM | GNP | 1999-02-16 | View |
| 510(k) | K981729 | IS-RUBELLA IGG TEST SYSTEM | LFX | 1999-01-28 | View |
| 510(k) | K981306 | DIAMEDIX IS-HSV 1 & 2 IGG TEST SYSTEM | LGC | 1998-09-29 | View |
No matching devices.
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