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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name nebulizer (direct patient interface)
510(k) Number K896696
Device Name (HEART) NEBULIZER
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
3941 J STREET, SUITE 354
SACRAMENTO,  CA  95819
Applicant Contact WONG, MD
Correspondent
VORTRAN MEDICAL TECHNOLOGY 1, INC.
3941 J STREET, SUITE 354
SACRAMENTO,  CA  95819
Correspondent Contact WONG, MD
Regulation Number868.5630
Classification Product Code
CAF  
Date Received11/28/1989
Decision Date 02/12/1990
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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