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R2 Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K102908	NOFACT IX	GJT	2011-12-19	View
510(k)	K102851	NOFACT VIII	GJT	2011-12-19	View
510(k)	K090105	LUPOTEK KCT	GGW	2010-12-30	View
510(k)	K083878	LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA	GIR	2010-06-25	View
510(k)	K082631	THROMBO TEK PSE, MODEL 90-480	GGP	2008-12-17	View
510(k)	K062306	PLASMACON N, PLASMACON L-1, PLASMACON L-2	GGC	2007-03-16	View
510(k)	K050817	T-TEK	GJA	2005-12-12	View
510(k)	K042919	FIBROTEK FIB	GIS	2004-11-29	View
510(k)	K040296	PHOSPHOPLASTIN RL	GJS	2004-05-24	View
510(k)	K033471	PHOSPHOLIN ES AND CALCIUM CHLORIDE	GGW	2004-02-04	View

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