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FDA 510(k)

Nuubo Smart

K-Number: K231620 · 2023-08-01

ApplicantSmart Solutions Technologies SL
Decision Date2023-08-01
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Nuubo Smart is a medical device manufactured by Smart Solutions Technologies SL. It received FDA 510(k) clearance on 2023-08-01 under approval number K231620. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nuubo Smart?

Nuubo Smart is a medical device that received FDA 510(k) clearance on 2023-08-01. It is manufactured by Smart Solutions Technologies SL. The 510(k) number is K231620.

When was Nuubo Smart approved by the FDA?

Nuubo Smart received FDA 510(k) clearance on 2023-08-01, under approval number K231620.

What company makes Nuubo Smart?

Nuubo Smart is manufactured by Smart Solutions Technologies SL.

What is the FDA product code for Nuubo Smart?

The FDA product code for Nuubo Smart is DQK.

Other Devices by Smart Solutions Technologies SL

K173461ECG recorder and Arrhythmia Detector

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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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