FDA 510(k) Applications Submitted by SUZAN ONEL

FDA 510(k) Number Submission Date Device Name Applicant
K040031 01/08/2004 CERAGEM-C THERMAL ACUPRESSURE MASSAGER CERAGEM CO., LTD.
K100720 03/15/2010 K-SHIELD PORT ACCESS INFUSION SET WITH HIGH PRESSURE TUBING KAWASUMI LABORATORIES, INC.
K061197 04/28/2006 KAWASUMI LABORATORIES EMPTY SOLUTION CONTAINER KAWASUMI LABORATORIES, INC.
K953823 08/15/1995 ARTERIAL VENOUS BLOOD TUBING SET MEDISYSTEMS CORP.
K112868 09/30/2011 DREAMGARD REM-SOFT, DREAMGARD REM-LITE, DREAMGARD REM-ULTRA, DREAMGARD REM-MAX DREAMGARD, INC.


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