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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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