Organon, Inc.

FDA 510(k) & PMA Approved Devices — 41 products

Total Devices41

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K950861	RECONSTITUTION ACCESSOREIS	FPK	1995-05-26	View
510(k)	K853388	MONOSTICON UNI-DOT	KTN	1985-08-22	View
510(k)	K842314	DUOCLON COLOR-CEPT	JHJ	1984-08-24	View
510(k)	K841525	OREIA II B-HCG PREGNANCY TEST KIT	JHI	1984-06-05	View
510(k)	K841602	ACCURATE BETA 30 PREGNANCY TEST KIT	LCX	1984-05-22	View
510(k)	K840650	B-NEOCEPT 30	JHJ	1984-04-04	View
510(k)	K832801	OREIA II B-HCG, ENZYME INNUNOASSAY	JHI	1983-12-08	View
510(k)	K831339	NEO-PREGNOSTICON DUOCLON TUBE TEST	JHJ	1983-06-08	View
510(k)	K831109	DUOCLON SLIDE TEST	JHI	1983-06-02	View
510(k)	K823682	BETA FFIRM TEST	JHJ	1983-01-07	View
510(k)	K812967	ACCURATE BETA	JHJ	1981-11-06	View
510(k)	K812334	B-NEOCEPT	JHJ	1981-09-01	View
510(k)	K812261	ACCURATE I	JHJ	1981-08-31	View
510(k)	K811940	OREIA II, B-HCG	JHJ	1981-08-03	View
510(k)	K811941	NEOCEPT	JHJ	1981-07-27	View
510(k)	K802974	RAPI-DOT	JHJ	1980-12-19	View
510(k)	K802634	STERIGAGE EO ETHYL. OXIDE STERIL. INDIC.	JOJ	1980-12-11	View
510(k)	K802693	OREIA-Q-TY, ENZYME IMMUNOASSAY	KLI	1980-12-10	View
510(k)	K802464	OREAI-Q-TU TEST	KHQ	1980-10-31	View
510(k)	K802358	OREIA-Q-DIG	KXT	1980-10-10	View