FDA 510(k) Applications Submitted by IMMUNETECH CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K061979 07/13/2006 MODIFICATION TO MYALLERGY TEST IMMUNETECH CORPORATION
K020387 02/05/2002 MYALLERGYTEST SYSTEM IMMUNETECH CORPORATION
K021698 05/22/2002 MY ALLERGY TEST IMMUNETECH CORPORATION
K032251 07/22/2003 IMMUNETECH TOTAL IGE SYSTEM IMMUNETECH CORPORATION


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