Amedic USA

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K897120EQUIP COVERS, STERILEJanuary 4, 1990
K892070GENERAL IVT NEEDLE GUIDE KIT, STERILESeptember 5, 1989
K892071GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILEAugust 8, 1989
K892069EXTENDED COVERS, STERILEAugust 8, 1989
K892068TRT (ACUSON) NEEDLE GUIDE KIT, STERILEAugust 4, 1989
K871467BIOPSY NEEDLE GUIDE KIT, STERILEAugust 21, 1987
K871609ULTRASOUND TRANSDUCER SHEATHS, STERILEJuly 15, 1987
K871565ULTRASOUND TRANSDUCER GEL, STERILEJuly 15, 1987
K871503BIOPSY NEEDLE GUIDE KIT, STERILEJuly 10, 1987
K864219TRANSVAGINAL ULTRASOUND BIOPSY NEEDLE GUIDEMarch 27, 1987