510(k) K101788

GIRAFFE OMNIBED by Ohmeda Medical — Product Code FMZ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 21, 2010
Date Received
June 25, 2010
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Incubator, Neonatal
Device Class
Class II
Regulation Number
880.5400
Review Panel
HO
Submission Type