Kawasumi Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kawasumi Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH), K-Shield Advantage Port Access Infusion Set (PAIS), Kawasumi Laboratories Blood Drawing Kit (BDK) System
11
Total
11
Cleared
0
Denied
Kawasumi Laboratories, Inc. has 11 FDA 510(k) cleared general hospital devices. Based in Washington, US.
Historical record: 11 cleared submissions from 2002 to 2019.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Compliance Associates, Inc. and Regulatory Compliance Associates, Inc. (Rca).
FDA 510(k) Regulatory Record - Kawasumi Laboratories, Inc.
11 devices
Cleared
Jul 08, 2019
Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH)
General Hospital
131d
Cleared
May 02, 2019
K-Shield Advantage Port Access Infusion Set (PAIS)
General Hospital
85d
Cleared
Sep 28, 2018
Kawasumi Laboratories Blood Drawing Kit (BDK) System
General Hospital
367d
Cleared
Mar 07, 2013
K-SHIELD ADVANTAGE PORT ACCESS INFUSION SET (PAIS)
General Hospital
127d
Cleared
Nov 18, 2010
K-SHIELD PORT ACCESS INFUSION SET WITH HIGH PRESSURE TUBING
General Hospital
248d
Cleared
Nov 03, 2010
K-SHIELD ARTERIAL VENOUS FISTULA SET WITH ANTINEEDLE STICK PROTECTOR
General Hospital
26d
Cleared
Jan 25, 2008
KAWASUMI LABORATORIES LARGE WING SETS WITH ANTINEEDLE STICK PROTECTOR
General Hospital
67d
Cleared
Jun 30, 2006
KAWASUMI LABORATORIES EMPTY SOLUTION CONTAINER
General Hospital
63d
Cleared
Jun 06, 2006
K-SHIELD PORT ACCESS INFUSION SET
General Hospital
92d
Cleared
Feb 26, 2003
WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR
General Hospital
93d
Cleared
Sep 12, 2002
KAWASUMI LABORATORIES ANTINEEDLE STICK PROTECTOR FOR USE WITH PORT ACCESS...
General Hospital
76d