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Ventrex, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K061044	FEATHERLITE AQUA TOCODYNAMOMETER	HFM	2006-07-12	View
510(k)	K013477	TOCO LITE, MODEL TD-01	HFM	2002-01-17	View
510(k)	K964821	COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67	DQA	1997-07-16	View
510(k)	K925044	VENTREX ALLERGEN DISC	DHB	1993-05-14	View
510(k)	K924119	VENTREX ALLERGEN DISC	DHB	1992-11-30	View

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