Kawasumi Laboratories America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kawasumi Laboratories America, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Kawasumi Laboratories America, Inc. has 6 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 6 cleared submissions from 2000 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kawasumi Laboratories America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kawasumi Laboratories America, Inc.
6 devices
Cleared
Oct 21, 2010
K-SHIELD SMALL VEIN INFUSION / WINGED COLLECTION SET W/ ANTI NEEDLE STICK...
General Hospital
21d
Cleared
Apr 15, 2003
IV ADD-ON FILTER ADMINISTRATION SET WITH AND WITHOUT Y CONNECT OR NEEDLELESS...
General Hospital
69d
Cleared
Jul 21, 2000
KAWASUMI LABORATORIES IV ADMINISTRATION SET, PRIMARY
General Hospital
77d
Cleared
Jul 21, 2000
KAWASUMI LABORATORIES IV ADMINISTRATION SET, STANDARD
General Hospital
77d
Cleared
Jul 21, 2000
KAWASUMI LABORATORIES IV ADMINISTRATION SET WITH FILTER
General Hospital
77d
Cleared
May 19, 2000
KAWASUMI LABORATORY BLOOD DRAWING KIT
Hematology
49d