FDA 510(k) Applications for Medical Device Product Code "DTS"
(Sucker, Cardiotomy Return, Cardiopulmonary Bypass)

FDA 510(k) Number Applicant Device Name Decision Date
K982891 CALIFORNIA MEDICAL LABORATORIES, INC. CALIFORNIA MEDICAL LABORATORIES INC. STANDARD AND SMALL RIGID TIP SUCTION WANDS 09/30/1998
K053021 ESTECH, INC. ESTECH CLEARVIEW MV ATRIAL DEPRESSOR 01/26/2006
K963756 INTERNATIONAL BIOPHYSICS CORP. IBC CARDIAC SUCTION WARD 11/14/1997


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