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Company · US

Angiodynamics, Div. E-Z-Em, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1996. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
QEY	Mechanical Thrombolysis Catheter	3
DXT	Injector And Syringe, Angiographic	1
GDF	Guide, Needle, Surgical	1
KRA	Catheter, Continuous Flush	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jul 17, 1996	K961763	*PULSESPRAY INFUSION SYSTEM** Angiodynamics, Div. E-Z-Em, Inc.	QEY
Jun 16, 1995	K951509	*PULSESPRAY INFUSION SYSTEM** Angiodynamics, Div. E-Z-Em, Inc.	QEY
Jun 14, 1995	K951602	*PULSESPRAY INFUSION SYSTEM** Angiodynamics, Div. E-Z-Em, Inc.	KRA
May 17, 1995	K950907	*PULSESPRAY INFUSION SYSTEM** Angiodynamics, Div. E-Z-Em, Inc.	QEY
Dec 13, 1994	K933846	ANGIOGRAPHY SYRINGE KITS Angiodynamics, Div. E-Z-Em, Inc.	DXT
Sep 1, 1992	K923120	MICROGUIDE LESION MARKING SYSTEM Angiodynamics, Div. E-Z-Em, Inc.	GDF

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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