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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name connector, airway (extension)
510(k) Number K881849
Device Name BODAI M.D.D. ADAPTOR(TM)
Applicant
B & B MEDICAL TECHNOLOGIES, INC.
3569 RECYCLE RD., SUITE 16
RANCHO CORDOVA,  CA  95670
Applicant Contact W BRIGGS,III
Correspondent
B & B MEDICAL TECHNOLOGIES, INC.
3569 RECYCLE RD., SUITE 16
RANCHO CORDOVA,  CA  95670
Correspondent Contact W BRIGGS,III
Regulation Number868.5810
Classification Product Code
BZA  
Date Received05/02/1988
Decision Date 07/01/1988
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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