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FDA 510(k) Applications Submitted by MATTHEW THIE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060382
02/14/2006
FLO-RITE, MODEL 478-1; FLO-RITE II, MODEL 478-1; SIMPULSE II, MODEL 478-2S; NUMATIX, MODEL NCD401; SIMPULSE, MODEL 478-1
AMERIFLO CORP.
K041057
04/23/2004
FLO-RITE
AMERIFLO CORP.
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