Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)
K-Number: K260326 · 2026-07-28
Device Summary
Frequently Asked Questions
What is the Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)?
Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1) is a medical device that received FDA 510(k) clearance on 2026-07-28. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K260326.
When did Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1) receive FDA 510(k) clearance?
Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1) received FDA 510(k) clearance on 2026-07-28, under 510(k) number K260326.
Who is the listed applicant for Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)?
The FDA 510(k) record lists Datex-Ohmeda, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)?
The FDA product code for Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1) is FMZ.
Other records listing Datex-Ohmeda, Inc. 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: FMZ)
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.