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Diagnostica, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K002756	EASE-A-CULT	KHE	2001-02-23	View
510(k)	K823348	H. INFLUENZA B ANTISERA FOR CIE	GRP	1982-12-28	View
510(k)	K812434	DIAGNOSTIC KITS & KIT COMPONENTS	LHT	1981-09-23	View
510(k)	K800398	PARACONTROL ABNORMAL IMMUNOGLOBULIN CONT	DEW	1980-03-12	View
510(k)	K791283	ANTI-HUMAN LAMBDA SERUM	DEH	1979-11-27	View
510(k)	K791284	ANTI-HUMAN KAPPA SERUM	DFH	1979-11-27	View
510(k)	K791281	ANTI-HUMAN IGG SERUM	DEW	1979-11-27	View
510(k)	K791282	ANTI-HUMAN SERUM	DGQ	1979-10-17	View
510(k)	K791285	ANTI-HUMAN GLOBULINS	DEW	1979-10-17	View
510(k)	K790671	DERMATOPHYTIN O	JXB	1979-05-31	View
510(k)	K790672	ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU	JWT	1979-05-31	View
510(k)	K781710	BUFFER, COLLAGEN REAGENT AND DILUENT	JBX	1978-10-24	View

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