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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
510(k) Number K843599
Device Name OHMEDA MODEL 5200 CO2 MONITOR
Applicant
OHMEDA MEDICAL
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
OHMEDA MEDICAL
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.1400
Classification Product Code
CCK  
Date Received09/12/1984
Decision Date 10/04/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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