Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Aesku Diagnostics

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K132082	AESKULISA DGP-A, AESKULISA DGP-G,AESKULISA DGP-CHECK	MST	2013-12-05	View
510(k)	K120889	AESKUSLIDES ANA HEP-2	DHN	2012-10-15	View
510(k)	K091859	AESKU PR3	MOB	2010-06-03	View
510(k)	K091860	AESKULISA MPO, MODEL 30-7303US	MOB	2010-02-23	View
510(k)	K081251	MODIFICATION TO AESKULISA DS DNA G	LSW	2008-05-13	View
510(k)	K081104	AESKULISA ANA HEP-2, REF 30-7115US	LKJ	2008-05-02	View
510(k)	K052439	AESKULISA GLIA A AND AESKULISA GLIA G	MST	2006-02-07	View
510(k)	K041628	AESKULISA DS DNA G	LSW	2004-10-14	View
510(k)	K041753	AESKULISA ENA 6 S	LLL	2004-07-14	View

↑