510(k) K101778

GIRAFFE INCUBATOR by Ohmeda Medical — Product Code FMZ

K101778 is an FDA 510(k) premarket notification submitted by Ohmeda Medical for the device "GIRAFFE INCUBATOR". The FDA issued a decision of Substantially Equivalent on July 21, 2010. The device falls under product code FMZ (Incubator, Neonatal), a Class II device regulated under 21 CFR 880.5400. Ohmeda Medical has at least 10 other 510(k) clearances on record.

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