Aesku Diagnostics

FDA Regulatory Profile

Aesku Diagnostics appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 5, 2013.

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K132082AESKULISA DGP-A, AESKULISA DGP-G,AESKULISA DGP-CHECKDecember 5, 2013
K120889AESKUSLIDES ANA HEP-2October 15, 2012
K091859AESKU PR3June 3, 2010
K091860AESKULISA MPO, MODEL 30-7303USFebruary 23, 2010
K081251MODIFICATION TO AESKULISA DS DNA GMay 13, 2008
K081104AESKULISA ANA HEP-2, REF 30-7115USMay 2, 2008
K052439AESKULISA GLIA A AND AESKULISA GLIA GFebruary 7, 2006
K041628AESKULISA DS DNA GOctober 14, 2004
K041753AESKULISA ENA 6 SJuly 14, 2004