R2 Diagnostics, Inc.
10 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| NOFACT IX (K102908) | R2 Diagnostics, Inc. | 2011-12-19 |
| NOFACT VIII (K102851) | R2 Diagnostics, Inc. | 2011-12-19 |
| LUPOTEK KCT (K090105) | R2 Diagnostics, Inc. | 2010-12-30 |
| LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA (K083878) | R2 Diagnostics, Inc. | 2010-06-25 |
| THROMBO TEK PSE, MODEL 90-480 (K082631) | R2 Diagnostics, Inc. | 2008-12-17 |
| PLASMACON N, PLASMACON L-1, PLASMACON L-2 (K062306) | R2 Diagnostics, Inc. | 2007-03-16 |
| T-TEK (K050817) | R2 Diagnostics, Inc. | 2005-12-12 |
| FIBROTEK FIB (K042919) | R2 Diagnostics, Inc. | 2004-11-29 |
| PHOSPHOPLASTIN RL (K040296) | R2 Diagnostics, Inc. | 2004-05-24 |
| PHOSPHOLIN ES AND CALCIUM CHLORIDE (K033471) | R2 Diagnostics, Inc. | 2004-02-04 |
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