R2 Diagnostics, Inc.
R2 Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2011.
Top product codes for R2 Diagnostics, Inc.
Recent clearances by R2 Diagnostics, Inc.
- K102851 — NOFACT VIII
- K102908 — NOFACT IX
- K090105 — LUPOTEK KCT
- K083878 — LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA
- K082631 — THROMBO TEK PSE, MODEL 90-480
- K062306 — PLASMACON N, PLASMACON L-1, PLASMACON L-2
- K050817 — T-TEK
- K042919 — FIBROTEK FIB
- K040296 — PHOSPHOPLASTIN RL
- K033471 — PHOSPHOLIN ES AND CALCIUM CHLORIDE
Data sourced from openFDA. This site is unofficial and independent of the FDA.