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

MODIFICATION TO: GIRAFFE AND PANDA WARMER

K Number: K090697 · Decision Apr 16, 2009
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
91
Applicant Total
120
Review Days
30

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Basic Information

Device Name
MODIFICATION TO: GIRAFFE AND PANDA WARMER
K Number
K090697
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5130
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ohmeda Medical
Date Received
March 17, 2009
Decision Date
April 16, 2009
Product Code
FMT
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
FMT Warmer, Infant Radiant

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Other Clearances by Ohmeda Medical

K Number Device Name
K123309 GIRAFFE AND PANDA WARMERS
K101788 GIRAFFE OMNIBED
K101778 GIRAFFE INCUBATOR
K072157 MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)
K070377 GIRAFFE AND PANDA WARMER
K070210 GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM
K070247 GIRAFFE AND PANDA BAG AND MASK RESUSCITATION SYSTEM
K040068 BILIBLANKET PLUS HIGH OUTPUT PHOTOTHERAPY SYSTEM
K020543 OHMEDA MEDICAL GIRAFFE OMNIBED
K020547 OHMEDA MEDICAL GIRAFFE INCUBATOR
Search all 120 clearances from Ohmeda Medical →