Livento Press, Soprano 10, Soprano
K-Number: K192251 · 2020-01-15
ApplicantCendres+Metaux SA
Decision Date2020-01-15
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Livento Press, Soprano 10, Soprano is a medical device manufactured by Cendres+Metaux SA. It received FDA 510(k) clearance on 2020-01-15 under approval number K192251. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Livento Press, Soprano 10, Soprano?
Livento Press, Soprano 10, Soprano is a medical device that received FDA 510(k) clearance on 2020-01-15. It is manufactured by Cendres+Metaux SA. The 510(k) number is K192251.
When was Livento Press, Soprano 10, Soprano approved by the FDA?
Livento Press, Soprano 10, Soprano received FDA 510(k) clearance on 2020-01-15, under approval number K192251.
What company makes Livento Press, Soprano 10, Soprano?
Livento Press, Soprano 10, Soprano is manufactured by Cendres+Metaux SA.
What is the FDA product code for Livento Press, Soprano 10, Soprano?
The FDA product code for Livento Press, Soprano 10, Soprano is EIH.
Other Devices by Cendres+Metaux SA
Related Devices (Code: EIH)
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.