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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Attachment, Intermittent Mandatory Ventilation (Imv)
510(k) Number K760263
Device Name I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)
Applicant
FOREGGER
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
FOREGGER
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5955
Classification Product Code
CBO  
Date Received07/21/1976
Decision Date 08/04/1976
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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