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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Apnea, Facility Use
510(k) Number K820943
Device Name SYSTEM I INFANT MONITORING SYS
Applicant
Burr Engineering & Development Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Burr Engineering & Development Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.2377
Classification Product Code
FLS  
Date Received04/06/1982
Decision Date 05/03/1982
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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