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FDA 510(k)

Neurescue device

K-Number: K210358 · 2021-05-21

ApplicantNeurescue Aps
Decision Date2021-05-21
Product CodeMJN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Neurescue device is a medical device manufactured by Neurescue Aps. It received FDA 510(k) clearance on 2021-05-21 under approval number K210358. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Neurescue device?

Neurescue device is a medical device that received FDA 510(k) clearance on 2021-05-21. It is manufactured by Neurescue Aps. The 510(k) number is K210358.

When was Neurescue device approved by the FDA?

Neurescue device received FDA 510(k) clearance on 2021-05-21, under approval number K210358.

What company makes Neurescue device?

Neurescue device is manufactured by Neurescue Aps.

What is the FDA product code for Neurescue device?

The FDA product code for Neurescue device is MJN.

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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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