Milex Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K001545PIPET CURETJune 15, 2000
K904774INGLAT-O-BALLDecember 7, 1990
K904026INFLAT-O-BALLOctober 10, 1990
K900903KOPANS HOOKWIRE LESION LOCALIZATION NEEDLEMay 3, 1990
K882628ENDO C BRUSHJuly 25, 1988
K862410MILEX KEGEL PERINEAL EXERCISERJuly 31, 1986
K861385MILEX BARTHOLIN GLAND CATHETERJune 16, 1986
K760264CURETTE, PROPOSED TIS-U-TRAP, METALOctober 6, 1976