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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