FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)

K Number: K251663 · Decision Oct 22, 2025
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
84
Applicant Total
58
Review Days
145

Basic Information

Device Name
Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)
K Number
K251663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5400
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Datex-Ohmeda, Inc.
Date Received
May 30, 2025
Decision Date
October 22, 2025
Product Code
FMZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMZ Incubator, Neonatal

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Other Clearances by Datex-Ohmeda, Inc.

K Number Device Name
K213867 Carestation 750/750c
K210384 CARESCAPE R860
K172702 Tec 820, Tec 850
K172045 Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2
K170872 Aisys CS2
K151570 Carestation 620/650/650C
K142679 CARESCAPE R860
K143530 Aespire View
K140575 ENGSTROM CARESTATION, ENGSTROM PRO
K132530 GE DATEX-OHMEDA AISYS CS2 (AISYS CS^2)
Search all 58 clearances from Datex-Ohmeda, Inc. →