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Cirrus Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K921704	IMMULITE(R) FSH	CGJ	1992-06-09	View
510(k)	K920411	IMMULITE HLH	CEP	1992-03-11	View
510(k)	K914833	IMMULITE DIGOXIN	DPO	1991-11-22	View
510(k)	K911796	IMMULITE(TM) HCG	DHA	1991-06-20	View
510(k)	K910677	IMMULITE(TM) T-UPTAKE	CEE	1991-04-29	View
510(k)	K910261	IMMULITE(TM) TOTAL T4	KLI	1991-04-16	View
510(k)	K905648	CRP LIPID REAGENT TEST PACK	CHH	1991-03-06	View
510(k)	K905214	IMMULITE (TM) TOTAL T3	CDP	1991-02-01	View
510(k)	K905769	IMMULITE HS-TSH	JLW	1991-01-31	View
510(k)	K905215	IMMULITE (TM) AUTOMATED IMMUNOASSAY ANALYZER	JJQ	1991-01-11	View

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