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FDA 510(k) Applications Submitted by AESKU.DIAGNOSTICS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081104
04/18/2008
AESKULISA ANA HEP-2, REF 30-7115US
AESKU.DIAGNOSTICS
K081251
05/02/2008
MODIFICATION TO AESKULISA DS DNA G
AESKU.DIAGNOSTICS
K091859
06/19/2009
AESKU PR3
AESKU.DIAGNOSTICS
K091860
06/19/2009
AESKULISA MPO, MODEL 30-7303US
AESKU.DIAGNOSTICS
K132082
07/05/2013
AESKULISA DGP-A, AESKULISA DGP-G,AESKULISA DGP-CHECK
AESKU.DIAGNOSTICS
K041628
06/16/2004
AESKULISA DS DNA G
AESKU.DIAGNOSTICS
K041753
06/29/2004
AESKULISA ENA 6 S
AESKU.DIAGNOSTICS
K052439
09/06/2005
AESKULISA GLIA A AND AESKULISA GLIA G
AESKU.DIAGNOSTICS
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