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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 K822689
Device Name PORTABLE MONITORING & SCREENING SPIROM.
Applicant
Boehringer Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Boehringer Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.1850
Classification Product Code
BZK  
Date Received09/03/1982
Decision Date 07/12/1983
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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