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FDA 510(k)

Beagank 4T Plus

K-Number: K233010 · 2023-11-21

ApplicantBelega, Inc.
Decision Date2023-11-21
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Beagank 4T Plus is a medical device manufactured by Belega, Inc.. It received FDA 510(k) clearance on 2023-11-21 under approval number K233010. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Beagank 4T Plus?

Beagank 4T Plus is a medical device that received FDA 510(k) clearance on 2023-11-21. It is manufactured by Belega, Inc.. The 510(k) number is K233010.

When was Beagank 4T Plus approved by the FDA?

Beagank 4T Plus received FDA 510(k) clearance on 2023-11-21, under approval number K233010.

What company makes Beagank 4T Plus?

Beagank 4T Plus is manufactured by Belega, Inc..

What is the FDA product code for Beagank 4T Plus?

The FDA product code for Beagank 4T Plus is NFO.

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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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