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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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