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Cambridge Bioscience Corp.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K890281	HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES	LSR	1989-03-15	View
510(k)	K881894	ADENOCLONE(R)-TYPE 40/41 EIA DIAGNOSTIC TEST (48)	GOD	1988-07-08	View
510(k)	K873312	ADENOCLONE(TM)-IFA, ADENOVIRUS ANTIGEN TEST	GOD	1988-02-24	View
510(k)	K873082	ADENOCLONE(TM)-EIA ADENOVIRUS ANTIGEN TEST	GOD	1988-02-24	View
510(k)	K852969	ROTACLONE ROTAVIRUS DIAGNOSTIC KIT	LIQ	1985-11-05	View

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