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FDA 510(k)

ATTIVA

K-Number: K220505 · 2023-02-09

ApplicantItalian Engineering S.R.L.
Decision Date2023-02-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATTIVA is the device name listed in this FDA 510(k) record. The listed applicant is Italian Engineering S.R.L.. It received FDA 510(k) clearance on 2023-02-09 under 510(k) number K220505. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATTIVA?

ATTIVA is a medical device that received FDA 510(k) clearance on 2023-02-09. The listed applicant is Italian Engineering S.R.L.. The 510(k) number is K220505.

When did ATTIVA receive FDA 510(k) clearance?

ATTIVA received FDA 510(k) clearance on 2023-02-09, under 510(k) number K220505.

Who is the listed applicant for ATTIVA?

The FDA 510(k) record lists Italian Engineering S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATTIVA?

The FDA product code for ATTIVA is GEI.

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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.

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