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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 K873696
Device Name BODAI NEO2-SAFE(TM)
Applicant
B & B MEDICAL TECHNOLOGIES, INC.
P.O. BOX 1503
ORANGEVALE,  CA  95662
Applicant Contact BRIGGS III
Correspondent
B & B MEDICAL TECHNOLOGIES, INC.
P.O. BOX 1503
ORANGEVALE,  CA  95662
Correspondent Contact BRIGGS III
Regulation Number868.5810
Classification Product Code
BZA  
Date Received09/14/1987
Decision Date 04/14/1988
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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