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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name ventilator, non-continuous (respirator)
510(k) Number K072009
Device Name WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340
Applicant
WEINMANN GERATE FUR MEDIZIN GMBH + CO. KG
KRONSAALSWEG 40
HAMBURG,  DE 22525
Applicant Contact ECKHARDT ALBERS
Correspondent
WEINMANN GERATE FUR MEDIZIN GMBH + CO. KG
KRONSAALSWEG 40
HAMBURG,  DE 22525
Correspondent Contact ECKHARDT ALBERS
Regulation Number868.5905
Classification Product Code
BZD  
Date Received07/23/2007
Decision Date 12/14/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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