Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Sit Sordina Iort Technologies Spa. It received FDA 510(k) clearance on 2019-05-22 under approval 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. It is manufactured by Sit Sordina Iort Technologies Spa. The 510(k) number is K182374.

When was LIAC S approved by the FDA?

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

What company makes LIAC S?

LIAC S is manufactured by Sit Sordina Iort Technologies Spa.

What is the FDA product code for LIAC S?

The FDA product code for LIAC S is IYE.

Other Devices by Sit Sordina Iort Technologies Spa

K172961LIAC HWL

Related Devices (Code: IYE)

K162476Varian High Energy Linear AcceleratorVarian Medical Systems, Inc. K161400ImagingRing SystemMedphoton GmbH K162468ClearCheckRadformation K162355Raycast MammoRx Carbon Fibre Breast BoardOrfit Industries NV K162577Dosimetry Check Version 5 Release 1Math Resolutions, LLC K162265CushionCast Moldable CushionsIzi Medical Products, LLC

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.

↑