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FDA 510(k) Applications Submitted by HYPERION, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K022800
08/23/2002
VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM
HYPERION, INC.
K013213
09/26/2001
HYPERION VISIQUANT ANA TEST KIT
HYPERION, INC.
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