Medical Device Manufacturer · US , Englewood , CO

Cottrell, Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1990

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cottrell, Ltd. General Hospital ✕

8 devices

1-8 of 8

Cleared Sep 13, 1999

ENDO-SPOR PLUS / HYPROCIDE

General Hospital · 784d

Cleared May 18, 1998

General Hospital · 444d

Cleared Apr 04, 1996

PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR

General Hospital · 84d

Cleared Aug 07, 1995

PROTOUCH OVERGLOVE

General Hospital · 87d

Cleared Jul 03, 1995

PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR

General Hospital · 748d

Cleared Jun 20, 1995

General Hospital · 54d

Cleared Mar 06, 1995

PRO BARRIER(TM) TUBE SOX(TM)

General Hospital · 112d

Cleared Apr 04, 1990

PROVIEW SELF-SEALING STERILIZATION POUCH

General Hospital · 317d