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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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