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

GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM

K Number: K070210 · Decision Apr 20, 2007
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
99
Applicant Total
120
Review Days
88

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Basic Information

Device Name
GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM
K Number
K070210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5925
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ohmeda Medical
Date Received
January 22, 2007
Decision Date
April 20, 2007
Product Code
BTL
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BTL Ventilator, Emergency, Powered (Resuscitator)

Similar 510(k) Clearances

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Other Clearances by Ohmeda Medical

K Number Device Name
K123309 GIRAFFE AND PANDA WARMERS
K101788 GIRAFFE OMNIBED
K101778 GIRAFFE INCUBATOR
K090697 MODIFICATION TO: GIRAFFE AND PANDA WARMER
K072157 MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)
K070377 GIRAFFE AND PANDA WARMER
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 →