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FDA 510(k) Applications Submitted by MAXI-AIDS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K041778
07/01/2004
REIZEN TALKING BLOOD PRESSURE MONITOR, MODEL #SF860T
MAXI-AIDS, INC.
K960567
02/09/1996
HF MEGA EAR
MAXI-AIDS, INC.
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