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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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