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FDA 510(k)

Sonio Suspect

K-Number: K243614 · 2025-02-21

ApplicantSonio
Decision Date2025-02-21
Product CodePOK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Sonio Suspect is a medical device manufactured by Sonio. It received FDA 510(k) clearance on 2025-02-21 under approval number K243614. The device is classified under product code POK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sonio Suspect?

Sonio Suspect is a medical device that received FDA 510(k) clearance on 2025-02-21. It is manufactured by Sonio. The 510(k) number is K243614.

When was Sonio Suspect approved by the FDA?

Sonio Suspect received FDA 510(k) clearance on 2025-02-21, under approval number K243614.

What company makes Sonio Suspect?

Sonio Suspect is manufactured by Sonio.

What is the FDA product code for Sonio Suspect?

The FDA product code for Sonio Suspect is POK.

Other Devices by Sonio

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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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