Eusol-C
K-Number: K162013 · 2016-09-15
ApplicantAl.Chi.Mi.A. S.R.L
Decision Date2016-09-15
Product CodeLYX
DecisionSubstantially Equivalent
Device Summary
Eusol-C is a medical device manufactured by Al.Chi.Mi.A. S.R.L. It received FDA 510(k) clearance on 2016-09-15 under approval number K162013. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Eusol-C?
Eusol-C is a medical device that received FDA 510(k) clearance on 2016-09-15. It is manufactured by Al.Chi.Mi.A. S.R.L. The 510(k) number is K162013.
When was Eusol-C approved by the FDA?
Eusol-C received FDA 510(k) clearance on 2016-09-15, under approval number K162013.
What company makes Eusol-C?
Eusol-C is manufactured by Al.Chi.Mi.A. S.R.L.
What is the FDA product code for Eusol-C?
The FDA product code for Eusol-C is LYX.
Other Devices by Al.Chi.Mi.A. S.R.L
Related Devices (Code: LYX)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.