Atlas FDA

GIRAFFE INCUBATOR

FDA 510(k) clearance K101778 · decided 2010-07-21

Clearance details

K-number
K101778
Device name
GIRAFFE INCUBATOR
Applicant
Ohmeda Medical
Decision
Substantially Equivalent
Date received
2010-06-25
Decision date
2010-07-21
Days to decision
26 days
Clearance type
Special
Product code
FMZ
Device class
2
Regulation number
880.5400
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Laurel, MD, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1) (K260326)Datex-Ohmeda, Inc.2026-07-28
Babyleo TN500 (K251619)Drägerwerk AG & Co. KGaA2026-02-13
Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1) (K251663)Datex-Ohmeda, Inc.2025-10-22
mOm Essential Incubator (ME1) (K243437)Mom Incubators Limited2025-08-14
Giraffe Incubator Carestation CS1 (K213553)Datex Ohmeda, Inc.2022-03-02
Infant Incubator (K190494)Ningbo David Medical Device Co., Ltd.2019-11-25
Babyleo TN500 (K182859)Dragerwerk AG & CO Kgaa2019-02-22
Isolette 8000 Plus (K182977)Draeger Medical Systems, Inc.2018-11-21
Isolette 8000 plus (K172154)Draeger Medical Sytems, Inc.2018-04-19
Babyleo TN500 (K162821)Draegerwerk AG & CO Kgaa2017-06-23
Giraffe OmniBed Carestation CS1 (K152814)Ohmeda Medical, A Division of Datex-Ohmeda,Inc. A GE Company2016-03-17
Giraffe Incubator Carestation CS1 (K152809)Ohmeda Medical, A Division of Datex-Ohmeda, Inc.2015-12-31

Recalls involving this device

RecordFirmDate
Giraffe OmniBed and Giraffe Incubator p/n 6600-0723-700 (rev A and B) labeled in part: *** recall (Z-1051-2013)GE Healthcare, LLC2013-04-05