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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