Ohmeda Medical Giraffe Incubator

FDA 510(k) K020547 · Ohmeda Medical

Substantially Equivalent

510(k) numberK020547

Submission

Device name
Ohmeda Medical Giraffe Incubator
Applicant
Ohmeda Medical
Laurel, MD, US
Received
February 19, 2002
Decision date
May 9, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMZ – Incubator, Neonatal
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5400
Specialty
General Hospital

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K101778Giraffe IncubatorFMZ · Special 07/21/2010SE
K090697Modification to: Giraffe and Panda WarmerFMT · Special 04/16/2009SE
K072157Modification to Giraffe and Panda Warmers (Giraffe and Panda Uninterruptible Power Supply)FMT · Special 08/27/2007SE
K070377Giraffe and Panda WarmerFMT · Traditional 07/11/2007SE
K070247Giraffe and Panda Bag and Mask Resuscitation SystemBTM · Traditional 04/20/2007SE
K070210Giraffe and Panda T- Piece Resuscitation SystemBTL · Traditional 04/20/2007SE
K040068Biliblanket Plus High Output Phototherapy SystemFMZ · Traditional 04/16/2004SE
K020543Ohmeda Medical Giraffe OmnibedFMZ · Traditional 05/09/2002SE

Questions and answers

When was Ohmeda Medical Giraffe Incubator cleared by the FDA?

Ohmeda Medical Giraffe Incubator (K020547) received a 510(k) decision of Substantially Equivalent on May 9, 2002, 79 days after the submission was received.

What is the product code of K020547?

The FDA product code is FMZ – Incubator, Neonatal, a Class II (moderate risk) device regulated under 21 CFR 880.5400.