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California Integrated Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K904095	HERPES SIMPLEX VIRUS TISSUE CULTURE CONF. TYPING	GQL	1991-02-01	View
510(k)	K874259	TRICHOMONAS DIRECT ENZYME IMMUNOASSAY	JWZ	1987-12-07	View
510(k)	K871278	MODIFIED CHLAMYDIA DIRECT SPECIMEN TEST KIT	LJP	1987-04-08	View
510(k)	K871279	MODIFIED TRICHOMONAS DIRECT SPECIMEN TEST KIT	JWZ	1987-04-08	View

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