Medical Device Manufacturer · US , Lakewood , CO

C.G.H. Medical, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1991

Total

Cleared

Denied

C.G.H. Medical, Inc. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Lakewood, US.

Historical record: 11 cleared submissions from 1991 to 1995.

Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - C.G.H. Medical, Inc.

11 devices

1-11 of 11

Cleared May 12, 1995

COBE CENTRYSYSTEM CS500 DIALYZER

K941708 · FJI

Gastroenterology & Urology · 401d

Cleared Jan 25, 1995

GAMBRO POLYFLUX II HEMODIALYZERIALYZER HEMODIAFILTER

K933818 · KDI

Gastroenterology & Urology · 539d

Cleared Sep 30, 1994

CENTRYSYSTEM 3 WITH CHARTS/BP OPTION

K925522 · KOC

Gastroenterology & Urology · 697d

Cleared Aug 05, 1994

FILTRAL HEMODIALYZERS

K920757 · KDI

Gastroenterology & Urology · 898d

Cleared Jul 07, 1994

LUNDIA ALPHA 700 HEMODIALYZER

K931720 · KDI

Gastroenterology & Urology · 456d

Cleared Jun 27, 1994

HEMOSPAL KIT B22 / MULTIFLOW 60 KIT

K924437 · KDI

Gastroenterology & Urology · 664d

Cleared Mar 22, 1994

GAMBRO BICART 720G

K940601 · KPO

Gastroenterology & Urology · 40d

Cleared May 27, 1992

GAMBRO ENGSTROM Y FILTER PKG. ALONE W/ VAR.MODELS

K915154 · CAN

Anesthesiology · 195d

Cleared Apr 13, 1992

GAMBRO ENGSTROM Y-FILTER WITH EDITH FLEX (1500F)

K914271 · CAN

Anesthesiology · 202d

Cleared Mar 06, 1992

GAMBRO LUNDIA ALPHA HEMODIALYZERS

K915504 · FJG

Gastroenterology & Urology · 88d

Cleared Aug 07, 1991

HEMOSPAL KIT B22

K911603 · KDI

Gastroenterology & Urology · 119d

C.G.H. Medical, Inc. - FDA 510(k) Cleared Devices

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