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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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