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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 K113801
Device Name VPAP ADAPT
Applicant
ResMed Corp
9001 Spectrum Center Blvd.
San Diego,  CA  92123
Applicant Contact DAVID D D'CRUZ
Correspondent
ResMed Corp
9001 Spectrum Center Blvd.
San Diego,  CA  92123
Correspondent Contact DAVID D D'CRUZ
Regulation Number868.5905
Classification Product Code
BZD  
Date Received12/22/2011
Decision Date 05/25/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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