Cottrell, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972708ENDO-SPOR PLUS / HYPROCIDESeptember 13, 1999
K970726VAPOCIDEMay 18, 1998
K960089PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATORApril 4, 1996
K952241PROTOUCH OVERGLOVEAugust 7, 1995
K952234BARRIER ALL FILMJuly 31, 1995
K932922PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATORJuly 3, 1995
K951983IMNI-IIJune 20, 1995
K945575PRO BARRIER(TM) TUBE SOX(TM)March 6, 1995
K893802PROVIEW SELF-SEALING STERILIZATION POUCHApril 4, 1990