FDA 510(k) Applications Submitted by SASCHA PFEIFFER

FDA 510(k) Number Submission Date Device Name Applicant
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


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