Critical Device Corp. is one of 6936 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Critical Device Corp. - FDA 510(k) Cleared Devices
Recent clearances: NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER WITH POSIFLOW POSITIVE DISPLACEMENT FEATURE, AND I.V. SETS, CDC VIAL AND BAG ACCESS PIN (CDC-P-1/P-2/P-3/P-4/P-5), NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER AND I.V. SET
6
Total
6
Cleared
0
Denied
Critical Device Corp. has 6 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 6 cleared submissions from 1996 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Critical Device Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Critical Device Corp.
6 devices
Cleared
Jan 20, 1999
MPS GRAVITY FLOW CONTROL SET
General Hospital
76d
Cleared
Apr 14, 1997
NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER WITH POSIFLOW POSITIVE...
General Hospital
126d
Cleared
Apr 02, 1997
CDC VIAL AND BAG ACCESS PIN (CDC-P-1/P-2/P-3/P-4/P-5)
General Hospital
110d
Cleared
Feb 10, 1997
NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER AND I.V. SET
General Hospital
73d
Cleared
Feb 16, 1996
NIMA (NEEDLELESS INJECTIONSITE MASTER ADAPTER) & I.V. SET
General Hospital
240d
Cleared
Feb 06, 1996
MACROBORE TUBING - CDC-F-1 THROUGH CDC-F-11
General Hospital
39d