Medical Device Manufacturer · US , Gurnee , IL

Opticon Medical, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1990

7

Total

7

Cleared

0

Denied

Opticon Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Gurnee, US.

Historical record: 7 cleared submissions from 1990 to 2004. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Opticon Medical, Inc.

7 devices

1-7 of 7

Cleared Jan 09, 2004

OPTION-VF URINARY CATHETER WITH ADAPTOR, MODEL FVA14218

Gastroenterology & Urology · 30d

Cleared Mar 19, 2003

OPTION-VF URINARY CATHETER, FV14218

Gastroenterology & Urology · 183d

Cleared May 16, 1997

OPTICON DIRECT MALE URINARY CATHETER FOR CONTINUOUS DRAINAGE

Gastroenterology & Urology · 78d

Cleared Sep 22, 1993

HEMOSTASIS VALVE AND TUBING SET

Cardiovascular · 251d

Cleared Jan 26, 1993

WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE

Anesthesiology · 812d

Cleared Feb 22, 1990

LOPER CELIAC PLEXUS BLOCK CATHETER KIT

Anesthesiology · 134d

Cleared Jan 19, 1990

OPTION EPIDURAL CATHETERS

Anesthesiology · 130d