Pro-Lab, Inc.

FDA 510(k) & PMA Approved Devices — 27 products

Total Devices27

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K934383	PROLEX (STREPTOCCAL GROUPING LATEX KIT)	GTZ	1995-01-27	View
510(k)	K914419	AMNIOTEST(TM)	HIO	1993-09-01	View
510(k)	K921421	LEGIONELLA REAGENS FOR DIRECT FLUORESCENT ANTIBODY	LHL	1992-07-28	View
510(k)	K903714	E. COLI 0157 LATEX TEST	GNA	1991-01-24	View
510(k)	K894221	ROSCO PYRR	JTO	1989-09-28	View
510(k)	K883995	X-ACT UREA/TDA	JSE	1988-10-12	View
510(k)	K883996	X-ACT LDC/IND	JSE	1988-10-12	View
510(k)	K871121	PROTECT T.M.	JTR	1987-04-14	View
510(k)	K870117	NEISSERIA/BRANHAMELLA DIFFERENTIAL TEST	JSX	1987-03-20	View
510(k)	K861142	MASTER KIT B	LRP	1986-07-10	View
510(k)	K861888	HIPPURATE HYDROLYSIS TEST	JTO	1986-06-03	View
510(k)	K861889	D'ALA RAPID TEST	JTO	1986-06-03	View
510(k)	K850246	MASTER KIT A		1985-04-09	View
510(k)	K850302	SUPLEX & SUPLEX DILUENT	JSK	1985-03-22	View
510(k)	K850299	C.N.V.T.	JSK	1985-03-20	View
510(k)	K850301	YEAST DIALYSATE	JSK	1985-03-20	View
510(k)	K850307	CAMPYLOBACTER SUPPLEMENT-BLASER/WANG	JSK	1985-03-20	View
510(k)	K850308	C.L.A.T.	JSK	1985-03-20	View
510(k)	K850306	CAMPYLOBACTER SUPPLEMENT -SKIRROW	JSK	1985-03-20	View
510(k)	K850300	MUCOLYSE	JSK	1985-03-20	View