FDA 510(k) Applications Submitted by AESKU, INC

FDA 510(k) Number Submission Date Device Name Applicant
K062217 08/01/2006 AESKULSKA BETA2-GLYCO-A AESKU, INC
K040463 02/23/2004 AESKULISA CARDIOLIPIN AGM AESKU, INC
K040953 04/12/2004 AESKULISA ANA HEP-2 AESKU, INC
K032469 08/11/2003 AESKULISA ANA 8PRO AESKU, INC
K042644 09/27/2004 AESKULISA TTG A AND AESKULISA TTG G AESKU, INC


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