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FDA 510(k)

ADAS 3D

K-Number: K240791 · 2024-09-09

ApplicantAdas3D Medical S.L.
Decision Date2024-09-09
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADAS 3D is a medical device manufactured by Adas3D Medical S.L.. It received FDA 510(k) clearance on 2024-09-09 under approval number K240791. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAS 3D?

ADAS 3D is a medical device that received FDA 510(k) clearance on 2024-09-09. It is manufactured by Adas3D Medical S.L.. The 510(k) number is K240791.

When was ADAS 3D approved by the FDA?

ADAS 3D received FDA 510(k) clearance on 2024-09-09, under approval number K240791.

What company makes ADAS 3D?

ADAS 3D is manufactured by Adas3D Medical S.L..

What is the FDA product code for ADAS 3D?

The FDA product code for ADAS 3D is QIH.

Other Devices by Adas3D Medical S.L.

K212421ADAS 3D K210850ADAS 3D K230803ADAS 3D

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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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