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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name mouthpiece, breathing
510(k) Number K810793
Device Name MOUTHPIECE, BREATHING
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5620
Classification Product Code
BYP  
Date Received03/23/1981
Decision Date 05/05/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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