FDA 510(k)

LIAC S

K-Number: K182374 · 2019-05-22

ApplicantSit Sordina Iort Technologies Spa

Decision Date2019-05-22

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

LIAC S is the device name listed in this FDA 510(k) record. The listed applicant is Sit Sordina Iort Technologies Spa. It received FDA 510(k) clearance on 2019-05-22 under 510(k) number K182374. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIAC S?

LIAC S is a medical device that received FDA 510(k) clearance on 2019-05-22. The listed applicant is Sit Sordina Iort Technologies Spa. The 510(k) number is K182374.

When did LIAC S receive FDA 510(k) clearance?

LIAC S received FDA 510(k) clearance on 2019-05-22, under 510(k) number K182374.

Who is the listed applicant for LIAC S?

The FDA 510(k) record lists Sit Sordina Iort Technologies Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIAC S?

The FDA product code for LIAC S is IYE.

Other records listing Sit Sordina Iort Technologies Spa 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.

K172961LIAC HWL

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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.