Cottrell, Ltd.

Cottrell, Ltd. holds 9 FDA 510(k) medical device clearances, first cleared 1990, most recent 1999.

Top product codes for Cottrell, Ltd.

Recent clearances by Cottrell, Ltd.

K972708 — ENDO-SPOR PLUS / HYPROCIDECode MED·1999-09-13
K970726 — VAPOCIDECode MED·1998-05-18
K960089 — PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATORCode JOJ·1996-04-04
K952241 — PROTOUCH OVERGLOVECode MMP·1995-08-07
K952234 — BARRIER ALL FILMCode EFS·1995-07-31
K932922 — PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATORCode MED·1995-07-03
K951983 — IMNI-IICode LRJ·1995-06-20
K945575 — PRO BARRIER(TM) TUBE SOX(TM)Code MMN·1995-03-06
K893802 — PROVIEW SELF-SEALING STERILIZATION POUCHCode KCT·1990-04-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.