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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Spirometer, Monitoring (W/Wo Alarm)
510(k) Number K921717
Device Name BICORE SMARTVALVE OCCLUSION VALVE
Applicant
Bicore Monitoring Systems
2 Faraday
Irvine,  CA  92718
Applicant Contact MUIR S MEINHOLD
Correspondent
Bicore Monitoring Systems
2 Faraday
Irvine,  CA  92718
Correspondent Contact MUIR S MEINHOLD
Regulation Number868.1850
Classification Product Code
BZK  
Date Received04/09/1992
Decision Date 11/06/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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