FDA 510(k) Applications Submitted by OEMEDIC INTERNATIONAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K021442 05/06/2002 OEMEDIC INTERNATIONAL INC. BESMED SINGLE USE ADULT, CHILD, INFANT MANUAL RESUSCITATOR WITH MASK & RESERVOIR OEMEDIC INTERNATIONAL, INC.
K021446 05/06/2002 OEMEDIC INTERNATIONAL INC. BESMED SILICONE ADULT, CHILD, INFANT MANUAL RESUSCITATOR WITH MASK AND RESERVOIR OEMEDIC INTERNATIONAL, INC.


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