Churchill Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Churchill Corp. - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
Churchill Corp. has 35 FDA 510(k) cleared general hospital devices. Based in Pineville, US.
Historical record: 35 cleared submissions from 1985 to 1988.
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 Corp.
35 devices
Cleared
Apr 14, 1988
CHURCHILL 0.22 MICRON LIQUID FILTER SETS
General Hospital
100d
Cleared
Apr 14, 1988
CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETS
General Hospital
100d
Cleared
Apr 14, 1988
ENTERAL BAG/SET
Gastroenterology & Urology
99d
Cleared
Apr 13, 1988
CHURCHILL 1.2 MICRON LIQUID FILTER SET
General Hospital
99d
Cleared
Oct 15, 1987
CHURCHILL PARENTERAL NUTRITION BAG - EVA
General Hospital
258d
Cleared
Oct 15, 1987
CHURCHILL-CATH
General Hospital
106d
Cleared
Oct 13, 1987
CHURCHILL ALBUMIN IV ADMINISTRATION SET
General Hospital
134d
Cleared
Oct 09, 1987
CHURCHILL TPN ADMINISTRATION SET
General Hospital
130d
Cleared
Sep 30, 1987
CHURCHILL INTER-CARDIAC SUCKER
Cardiovascular
126d
Cleared
Jul 16, 1987
NITROGLYCERINE PUMP SET
General Hospital
120d
Cleared
Jun 15, 1987
EXTENSION TUBE PUMP SET
General Hospital
89d
Cleared
Jun 15, 1987
IV PUMP SET
General Hospital
89d