FDA 510(k)

SMART FINDER

K-Number: K203509 · 2021-07-14

Decision Date2021-07-14

Product CodeIZH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SMART FINDER is the device name listed in this FDA 510(k) record. The listed applicant is Ims Giotto S.P.A.. It received FDA 510(k) clearance on 2021-07-14 under 510(k) 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. The listed applicant is Ims Giotto S.P.A.. The 510(k) number is K203509.

When did SMART FINDER receive FDA 510(k) clearance?

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

Who is the listed applicant for SMART FINDER?

The FDA 510(k) record lists Ims Giotto S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMART FINDER?

The FDA product code for SMART FINDER is IZH.

Other records listing Ims Giotto S.P.A. 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.

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

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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.