Dymax Corp

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
7
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K032135SITE-RITE IV ULTRASOUND SYSTEMJuly 21, 2003
K993624SITE-RITE 3 ULTRASOUND SYSTEMNovember 10, 1999
K931403SITERITE NEEDLE GUIDE (MODIFIED)July 27, 1993
K903158SITERITE NEEDLE GUIDESeptember 27, 1990
K894415DYMAX ENDOVAGINAL BIOPSY GUIDEOctober 25, 1989
K862127DYMAX PERSONAL SCANNERDecember 11, 1986
K850478PLUS 1April 15, 1985