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

OHMEDA 5500 AIRWAY PRESSURE MONITOR

K Number: K864536 · Decision Jan 12, 1987
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
120
Review Days
56

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Basic Information

Device Name
OHMEDA 5500 AIRWAY PRESSURE MONITOR
K Number
K864536
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Ohmeda Medical
Date Received
November 17, 1986
Decision Date
January 12, 1987
Product Code
CAP
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
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

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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
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
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