FDA 510(k) Applications Submitted by R2 DIAGNOSTICS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K062306 |
08/08/2006 |
PLASMACON N, PLASMACON L-1, PLASMACON L-2 |
R2 DIAGNOSTICS, INC. |
| K090105 |
01/15/2009 |
LUPOTEK KCT |
R2 DIAGNOSTICS, INC. |
| K082631 |
09/10/2008 |
THROMBO TEK PSE, MODEL 90-480 |
R2 DIAGNOSTICS, INC. |
| K102851 |
09/29/2010 |
NOFACT VIII |
R2 DIAGNOSTICS, INC. |
| K102908 |
10/01/2010 |
NOFACT IX |
R2 DIAGNOSTICS, INC. |
| K083878 |
12/29/2008 |
LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA |
R2 DIAGNOSTICS, INC. |
| K040296 |
02/09/2004 |
PHOSPHOPLASTIN RL |
R2 DIAGNOSTICS, INC. |
| K050817 |
03/31/2005 |
T-TEK |
R2 DIAGNOSTICS, INC. |
| K042919 |
10/22/2004 |
FIBROTEK FIB |
R2 DIAGNOSTICS, INC. |
| K033471 |
11/03/2003 |
PHOSPHOLIN ES AND CALCIUM CHLORIDE |
R2 DIAGNOSTICS, INC. |
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