Medical Device Manufacturer · US , Englewood , CO

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

9 submissions · 9 cleared · Since 1990

Total

Cleared

Denied

Cottrell, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Englewood, US.

Historical record: 9 cleared submissions from 1990 to 1999. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Cottrell, Ltd. Filter by specialty or product code using the sidebar.

Cottrell, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

9 devices

1-9 of 9

Cleared Sep 13, 1999

ENDO-SPOR PLUS / HYPROCIDE

K972708 · MED

General Hospital · 784d

Cleared May 18, 1998

VAPOCIDE

K970726 · MED

General Hospital · 444d

Cleared Apr 04, 1996

PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR

K960089 · JOJ

General Hospital · 84d

Cleared Aug 07, 1995

PROTOUCH OVERGLOVE

K952241 · MMP

General Hospital · 87d

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

K932922 · MED

General Hospital · 748d

Cleared Jun 20, 1995

IMNI-II

K951983 · LRJ

General Hospital · 54d

Cleared Mar 06, 1995

PRO BARRIER(TM) TUBE SOX(TM)

K945575 · MMN

General Hospital · 112d

Cleared Apr 04, 1990

PROVIEW SELF-SEALING STERILIZATION POUCH

K893802 · KCT

General Hospital · 317d

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

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

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