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Wien Laboratories, Inc.

FDA 510(k) & PMA Approved Devices — 13 products

Total Devices13

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K912850	SHBG	CDZ	1991-08-12	View
510(k)	K834246	PROGESTERONE TEST SET 125I 17-OH	JLX	1984-02-04	View
510(k)	K832452	ANDROSTENEDIONE TEST SET 125I	CIZ	1983-09-12	View
510(k)	K823200	125 I-DEHYDROEPIANDROSTERONE SULFATE	JKC	1982-11-29	View
510(k)	K821653	PROTRIPTYLINE TRI-CY TEST SET	LFG	1982-06-14	View
510(k)	K821652	DOXEPIN TRI-CY TEST SET	LFG	1982-06-14	View
510(k)	K802728	125I-TESTOSTERONE TEST SET	CDZ	1980-12-11	View
510(k)	K792041	DHEA-SULFATE TEST SET	JKC	1979-10-30	View
510(k)	K781834	TEST SET, 125 I-DIGOXIN	DNL	1979-01-03	View
510(k)	K781599	I-ESTRIOL TEST SET	CGI	1978-10-17	View
510(k)	K772306	125I DIGOXIN TEST SET	DPB	1977-12-22	View
510(k)	K771793	DHEA TEST SET	CIY	1977-11-02	View
510(k)	K771729	17-HYDROXYPROGESTERONE TEST SET	JLX	1977-10-21	View

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