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FDA 510(k)

Leltek Ultrasound Imaging System (Model: LU700 Series)

K-Number: K222365 · 2022-10-25

ApplicantLeltek, Inc.
Decision Date2022-10-25
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Leltek Ultrasound Imaging System (Model: LU700 Series) is a medical device manufactured by Leltek, Inc.. It received FDA 510(k) clearance on 2022-10-25 under approval number K222365. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Leltek Ultrasound Imaging System (Model: LU700 Series)?

Leltek Ultrasound Imaging System (Model: LU700 Series) is a medical device that received FDA 510(k) clearance on 2022-10-25. It is manufactured by Leltek, Inc.. The 510(k) number is K222365.

When was Leltek Ultrasound Imaging System (Model: LU700 Series) approved by the FDA?

Leltek Ultrasound Imaging System (Model: LU700 Series) received FDA 510(k) clearance on 2022-10-25, under approval number K222365.

What company makes Leltek Ultrasound Imaging System (Model: LU700 Series)?

Leltek Ultrasound Imaging System (Model: LU700 Series) is manufactured by Leltek, Inc..

What is the FDA product code for Leltek Ultrasound Imaging System (Model: LU700 Series)?

The FDA product code for Leltek Ultrasound Imaging System (Model: LU700 Series) is IYN.

Related Clinical Trials

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Official Source

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