Medical Device Manufacturer · US , Englewood , CO

Denver Biomedicals, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1981

Total

Cleared

Denied

Denver Biomedicals, Inc. has 10 FDA 510(k) cleared medical devices. Based in Englewood, US.

Historical record: 10 cleared submissions from 1981 to 2005. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Denver Biomedicals, Inc.

10 devices

1-10 of 10

Cleared Jun 13, 2005

DENVER PLEURX DRAINAGE KIT AND DENVER PLEURX VACUUM BOTTLE WITH DRAINAGE LINE

K051084 · DWM

Anesthesiology · 46d

Cleared Jun 01, 2001

DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER

K011020 · KPM

Gastroenterology & Urology · 58d

Cleared Mar 20, 2001

PLEURX PLEURAL CATHETER AND DRAINAGE KITS

K010642 · DWM

Anesthesiology · 15d

Cleared Jan 02, 2001

DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES...

K003451 · KPM

Gastroenterology & Urology · 56d

Cleared Mar 01, 1995

TUNNELER

K943968 · MDM

General & Plastic Surgery · 198d

Cleared Feb 18, 1994

DENVER(R) PERITONEO-SUBCLAVIAN SHUNT

K913728 · KPM

Gastroenterology & Urology · 913d

Cleared Aug 27, 1984

THE DENVER PLEURAL-PERITONEAL SHUNT

K842139 · KPM

Gastroenterology & Urology · 89d

Cleared Sep 21, 1982

DENVER PERITONEO-VENOUS SHUNT (DP-VS)

K822686 · KPM

Gastroenterology & Urology · 18d

Cleared Aug 07, 1981

CROUCH CORNEAL PROTECTOR

K811577 · HOY

Ophthalmic · 63d

Cleared Jul 01, 1981

DENVER PERITONEO-VENOUS SHUNT

K811183 · KPM

Gastroenterology & Urology · 63d

Denver Biomedicals, Inc. - FDA 510(k) Cleared Devices

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