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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, Oxygen, Gaseous-Phase
510(k) Number K852823
Device Name DMA OXYGEN MONITOR
Applicant
Ferguson Medical
3407 Bay Ave.
Chico,  CA  95973 -8619
Applicant Contact FRANK FERGUSON
Correspondent
Ferguson Medical
3407 Bay Ave.
Chico,  CA  95973 -8619
Correspondent Contact FRANK FERGUSON
Regulation Number868.1720
Classification Product Code
CCL  
Date Received07/01/1985
Decision Date 10/29/1985
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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