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FDA 510(k)

SMART FINDER

K-Number: K203509 · 2021-07-14

ApplicantIms Giotto S.P.A.
Decision Date2021-07-14
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SMART FINDER is a medical device manufactured by Ims Giotto S.P.A.. It received FDA 510(k) clearance on 2021-07-14 under approval number K203509. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMART FINDER?

SMART FINDER is a medical device that received FDA 510(k) clearance on 2021-07-14. It is manufactured by Ims Giotto S.P.A.. The 510(k) number is K203509.

When was SMART FINDER approved by the FDA?

SMART FINDER received FDA 510(k) clearance on 2021-07-14, under approval number K203509.

What company makes SMART FINDER?

SMART FINDER is manufactured by Ims Giotto S.P.A..

What is the FDA product code for SMART FINDER?

The FDA product code for SMART FINDER is IZH.

Other Devices by Ims Giotto S.P.A.

K200424Giotto Class (Models - 3000X-YY and 4000X-YY)

Related Devices (Code: IZH)

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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.

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