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FDA 510(k) Applications Submitted by DRTECH CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080064
01/10/2008
FLAATZ 750
DRTECH CORP.
K091747
06/16/2009
FLAATZ 500
DRTECH CORP.
K102474
08/30/2010
FLAATZ 750E
DRTECH CORP.
K111583
06/07/2011
FLAATZ 560
DRTECH CORP.
K111655
06/13/2011
FLAATZ 760
DRTECH CORP.
K132842
09/10/2013
FLAATZ 600 SERIES (FLAATZ 600/601)
DRTECH CORP.
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