Churchill Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Churchill Medical Systems, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Churchill Medical Systems, Inc. has 12 FDA 510(k) cleared general hospital devices. Based in Horsham, US.
Historical record: 12 cleared submissions from 1988 to 2004.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Churchill Medical Systems, Inc.
12 devices
Cleared
Dec 21, 2004
CHURCHILL MEDICAL DUAL CHAMBER EMPTY CONTAINER
General Hospital
243d
Cleared
May 13, 2002
MODIFICATION TO 30 EXTENSION SET
General Hospital
11d
Cleared
Mar 27, 2002
UNIVERSAL VIAL ACCESS SPIKE WITH NEEDLELESS CONNECTOR
General Hospital
117d
Cleared
Mar 12, 2002
WING SAFE INFUSION SET 20 GA, SHS2000 SERIES
General Hospital
25d
Cleared
Jan 10, 2002
VENTED VIAL ACCESS DEVICE
General Hospital
41d
Cleared
Sep 11, 2001
CHURCHILL MEDICAL SYSTEMS STOPCOCK
General Hospital
62d
Cleared
Sep 10, 2001
PRESSURE ACTIVATED CHECK VALVE
General Hospital
84d
Cleared
Jun 12, 2001
PRIMARY SOLUTION SET WITH UNIVERSAL SPIKE, INJECTION SITE AND MALE LUER LOCK
General Hospital
41d
Cleared
Jan 11, 1990
CMS IV FILTERS
General Hospital
69d
Cleared
Nov 13, 1989
.22 & 1.2 MICRON IV FILTERS
General Hospital
101d
Cleared
Nov 07, 1988
CMS IV EXTENSION SETS
General Hospital
20d
Cleared
Aug 25, 1988
30 IV EXTENSION SET W/TWO MALE LUER LOCKS
General Hospital
69d