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FDA 510(k) Applications Submitted by DURTECH SYSTEM CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K053284
11/25/2005
MAGBODY DT-600
DURTECH SYSTEM CORP.
K053285
11/25/2005
MAGBODY DT-1200, DT-1200T, DT-1200M, DT-1200PT, DT-1200PM
DURTECH SYSTEM CORP.
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