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FDA 510(k) Applications Submitted by MAXTEC, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040484
02/25/2004
MAXO2+, MODEL A AND AE
MAXTEC, INC.
K063488
11/17/2006
MAXO2 CU
MAXTEC, INC.
K133540
11/18/2013
FLOCAP
MAXTEC, INC.
K113232
11/02/2011
MAXMIXING BLOCK
MAXTEC, INC.
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