Promedical , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K954596PRO-B CORE-RECT COAXIAL BIOPSY SYSTEMOctober 7, 1995
K952350JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN)July 17, 1995
K951598PRO-B BIOPSY NEEDLEApril 21, 1995
K944944CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLEDecember 21, 1994
K944942BREAST LESION LOCALIZATION NEEDLENovember 4, 1994