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Germaine Laboratories, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K051727	AIMSTICK URINE REAGENT STRIPS	CEN	2005-10-26	View
510(k)	K013857	AIMSTEP PREGNANCY	DHA	2002-01-22	View
510(k)	K991369	ACCUDIP HOME PREGNANCY AND/OR AIMSTICK PREGNANCY	LCX	1999-05-10	View
510(k)	K981165	AIMSTEP COMBO PREGNANCY, 1 TEST, 30 TEST, 50 TEST, 100 TEST	JHI	1998-04-16	View
510(k)	K980531	AIMSTEP PREGNANCY	JHI	1998-03-06	View
510(k)	K974368	AIMSTICK PBD PREGNANCY	DHA	1998-01-02	View
510(k)	K974512	AIMSTICK PBD COMBO PREGNANCY	DHA	1998-01-02	View
510(k)	K973825	MIDSTREAM HOME REGNANCY TEST	DHA	1997-12-19	View

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