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Dymax Corp

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K032135	SITE-RITE IV ULTRASOUND SYSTEM	IYO	2003-07-21	View
510(k)	K993624	SITE-RITE 3 ULTRASOUND SYSTEM	IYO	1999-11-10	View
510(k)	K931403	SITERITE NEEDLE GUIDE (MODIFIED)	DQY	1993-07-27	View
510(k)	K903158	SITERITE NEEDLE GUIDE	DQY	1990-09-27	View
510(k)	K894415	DYMAX ENDOVAGINAL BIOPSY GUIDE	HGL	1989-10-25	View
510(k)	K862127	DYMAX PERSONAL SCANNER	IYO	1986-12-11	View
510(k)	K850478	PLUS 1	IYO	1985-04-15	View

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