Eusol-C
K-Number: K162013 · 2016-09-15
Device Summary
Frequently Asked Questions
What is the Eusol-C?
Eusol-C is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Al.Chi.Mi.A. S.R.L. The 510(k) number is K162013.
When did Eusol-C receive FDA 510(k) clearance?
Eusol-C received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162013.
Who is the listed applicant for Eusol-C?
The FDA 510(k) record lists Al.Chi.Mi.A. S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Eusol-C?
The FDA product code for Eusol-C is LYX.
Other records listing Al.Chi.Mi.A. S.R.L as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LYX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.