Beagank 4T Plus
K-Number: K233010 · 2023-11-21
Device Summary
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. The listed applicant is Belega, Inc.. The 510(k) number is K233010.
When did Beagank 4T Plus receive FDA 510(k) clearance?
Beagank 4T Plus received FDA 510(k) clearance on 2023-11-21, under 510(k) number K233010.
Who is the listed applicant for Beagank 4T Plus?
The FDA 510(k) record lists Belega, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Beagank 4T Plus?
The FDA product code for Beagank 4T Plus is NFO.
Related Devices (Code: NFO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.