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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