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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 a medical device manufactured by Italian Engineering S.R.L.. It received FDA 510(k) clearance on 2023-02-09 under approval 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. It is manufactured by Italian Engineering S.R.L.. The 510(k) number is K220505.

When was ATTIVA approved by the FDA?

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

What company makes ATTIVA?

ATTIVA is manufactured by Italian Engineering S.R.L..

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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