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FDA 510(k)

Livento Press, Soprano 10, Soprano

K-Number: K192251 · 2020-01-15

Decision Date2020-01-15
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Livento Press, Soprano 10, Soprano is the device name listed in this FDA 510(k) record. The listed applicant is Cendres+Metaux SA. It received FDA 510(k) clearance on 2020-01-15 under 510(k) 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. The listed applicant is Cendres+Metaux SA. The 510(k) number is K192251.

When did Livento Press, Soprano 10, Soprano receive FDA 510(k) clearance?

Livento Press, Soprano 10, Soprano received FDA 510(k) clearance on 2020-01-15, under 510(k) number K192251.

Who is the listed applicant for Livento Press, Soprano 10, Soprano?

The FDA 510(k) record lists Cendres+Metaux SA as the applicant. This does not by itself establish the device manufacturer.

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 records listing Cendres+Metaux SA 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: EIH)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.