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

OHMEDA MODEL 5330 ANESTHETIC MONITOR

K Number: K931439 · Decision Oct 19, 1993
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
21
Applicant Total
120
Review Days
211

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Basic Information

Device Name
OHMEDA MODEL 5330 ANESTHETIC MONITOR
K Number
K931439
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1500
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ohmeda Medical
Date Received
March 22, 1993
Decision Date
October 19, 1993
Product Code
CBQ
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
CBQ Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)

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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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