Atlan
K-Number: K230931 · 2023-07-23
Device Summary
Frequently Asked Questions
What is the Atlan?
Atlan is a medical device that received FDA 510(k) clearance on 2023-07-23. The listed applicant is Drägerwerk AG Co. Kgaa. The 510(k) number is K230931.
When did Atlan receive FDA 510(k) clearance?
Atlan received FDA 510(k) clearance on 2023-07-23, under 510(k) number K230931.
Who is the listed applicant for Atlan?
The FDA 510(k) record lists Drägerwerk AG Co. Kgaa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Atlan?
The FDA product code for Atlan is BSZ.
Other records listing Drägerwerk AG Co. Kgaa as applicant
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.
Related Devices (Code: BSZ)
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.