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FDA 510(k) Applications Submitted by NEOMEDIX CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K024304
12/24/2002
MICROSURGICAL BIPOLAR HANDPIECE
NEOMEDIX CORP.
K040239
02/02/2004
SUPRAFLOW CONSOLE
NEOMEDIX CORP.
K040584
03/05/2004
NMX-1000
NEOMEDIX CORP.
K061258
05/05/2006
TRABECTOME HIGH FREQUENCY GENERATOR/LP
NEOMEDIX CORP.
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