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

FDA 510(k) Number Submission Date Device Name Applicant
K081355 05/14/2008 BIOFLEX LD-R100 TREATMENT HEAD MEDITECH INTERNATIONAL, INC.
K051875 07/11/2005 BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS MEDITECH INTERNATIONAL, INC.
K041885 07/12/2004 BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS MEDITECH INTERNATIONAL, INC.
K072551 09/10/2007 LD-I 75 AND LD-I 200 MEDITECH INTERNATIONAL, INC.
K023621 10/29/2002 BIOFLEX PROFESSIONAL THERAPY SYSTEM MEDITECH INTERNATIONAL, INC.


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