Giraffe Omnibed

FDA 510(k) K101788 · Ohmeda Medical

Substantially Equivalent

510(k) numberK101788

Submission

Device name
Giraffe Omnibed
Applicant
Ohmeda Medical
Laurel, MD, US
Received
June 25, 2010
Decision date
July 21, 2010
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMZ – Incubator, Neonatal
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5400
Specialty
General Hospital

Other 510(k)s with product code FMZ

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K260326Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)FMZ · Traditional Datex-Ohmeda, Inc.07/28/2026SE
K251619Babyleo TN500FMZ · Traditional Drägerwerk AG & Co. KGaA02/13/2026SE
K251663Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)FMZ · Traditional Datex-Ohmeda, Inc.10/22/2025SE
K243437mOm Essential Incubator (ME1)FMZ · Traditional Mom Incubators Limited08/14/2025SE
K213553Giraffe Incubator Carestation CS1FMZ · Traditional Datex Ohmeda, Inc.03/02/2022SE
K190494Infant IncubatorFMZ · Traditional Ningbo David Medical Device Co., Ltd.11/25/2019SE
K182859Babyleo TN500FMZ · Special Dragerwerk AG & CO Kgaa02/22/2019SE
K182977Isolette 8000 PlusFMZ · Special Draeger Medical Systems, Inc.11/21/2018SE
K172154Isolette 8000 plusFMZ · Traditional Draeger Medical Sytems, Inc.04/19/2018SE
K162821Babyleo TN500FMZ · Traditional Draegerwerk AG & CO Kgaa06/23/2017SE

More from Draegerwerk AG & CO Kgaa

510(k)DeviceDecision
K123309Giraffe and Panda WarmersFMT · Traditional 02/05/2013SE
K101778Giraffe IncubatorFMZ · Special 07/21/2010SE
K090697Modification to: Giraffe and Panda WarmerFMT · Special 04/16/2009SE
K072157Modification to Giraffe and Panda Warmers (Giraffe and Panda Uninterruptible Power Supply)FMT · Special 08/27/2007SE
K070377Giraffe and Panda WarmerFMT · Traditional 07/11/2007SE
K070247Giraffe and Panda Bag and Mask Resuscitation SystemBTM · Traditional 04/20/2007SE
K070210Giraffe and Panda T- Piece Resuscitation SystemBTL · Traditional 04/20/2007SE
K040068Biliblanket Plus High Output Phototherapy SystemFMZ · Traditional 04/16/2004SE
K020547Ohmeda Medical Giraffe IncubatorFMZ · Traditional 05/09/2002SE
K020543Ohmeda Medical Giraffe OmnibedFMZ · Traditional 05/09/2002SE

Questions and answers

When was Giraffe Omnibed cleared by the FDA?

Giraffe Omnibed (K101788) received a 510(k) decision of Substantially Equivalent on July 21, 2010, 26 days after the submission was received.

What is the product code of K101788?

The FDA product code is FMZ – Incubator, Neonatal, a Class II (moderate risk) device regulated under 21 CFR 880.5400.