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FDA 510(k)

Atlan

K-Number: K230931 · 2023-07-23

ApplicantDrägerwerk AG Co. Kgaa
Decision Date2023-07-23
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Atlan is a medical device manufactured by Drägerwerk AG Co. Kgaa. It received FDA 510(k) clearance on 2023-07-23 under approval number K230931. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Atlan?

Atlan is a medical device that received FDA 510(k) clearance on 2023-07-23. It is manufactured by Drägerwerk AG Co. Kgaa. The 510(k) number is K230931.

When was Atlan approved by the FDA?

Atlan received FDA 510(k) clearance on 2023-07-23, under approval number K230931.

What company makes Atlan?

Atlan is manufactured by Drägerwerk AG Co. Kgaa.

What is the FDA product code for Atlan?

The FDA product code for Atlan is BSZ.

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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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