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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Vaporizer, Anesthesia, Non-Heated
510(k) Number K810289
Device Name MODULUS VERNI-TROL ANESTHETIC VAPORIZER
Applicant
Ohio Medical Products
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Ohio Medical Products
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.5880
Classification Product Code
CAD  
Date Received02/02/1981
Decision Date 03/04/1981
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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