Orion Corp.

FDA 510(k) & PMA Approved Devices — 21 products

Total Devices21

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K912391	RUBALEX, MODIFICATION	LQN	1992-05-04	View
510(k)	K901637	RESUBMITTED MODIFIED RUBALEX	LQN	1990-04-26	View
510(k)	K884650	RESUBMITTED SCANORA	IZF	1989-03-16	View
510(k)	K890199	DENTOCULT SM-STRIP MUTANS	JSI	1989-03-02	View
510(k)	K881506	MAMEX DC MAG MG12	IZH	1988-06-10	View
510(k)	K881505	MAMEX DC MG11	IZH	1988-06-10	View
510(k)	K874040	MAMEX DC S SL10/MG14	IZH	1987-11-23	View
510(k)	K872744	MODIFIED CHLAMYSET ANTIGEN	LJP	1987-09-22	View
510(k)	K864457	CHLAMYSET ANTIBODY EIA	LJC	1987-09-11	View
510(k)	K872301	DENTOCULT-SM CULTURE-PADDLE	JSI	1987-09-11	View
510(k)	K872058	ORICULT-N CULTURE-PADDLE	JSI	1987-06-10	View
510(k)	K861882	IMMUNOCHEMICAL ASSAY APOLIPOPROTEIN B	MSJ	1986-10-29	View
510(k)	K861883	IMMUNOCHEMICAL ASSAY OF APOLIPOPROTEIN A1	MSJ	1986-10-29	View
510(k)	K863730	MYOLEX	DDR	1986-10-15	View
510(k)	K862671	MICROALBUMINURIA ASSAY	DCF	1986-09-18	View
510(k)	K860679	IMMUNOCHEMICAL ASSAY OF C-REACTIVE PROTEIN	DCN	1986-08-04	View
510(k)	K861881	RUBALEX (REVISED VERSION)	LQN	1986-06-04	View
510(k)	K853401	CHLAMYSET ANTIGEN	LJP	1986-04-28	View
510(k)	K852788	RUBALEX	LQN	1986-03-12	View
510(k)	K860529	ROTALEX	LIQ	1986-03-04	View