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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name tube, tympanostomy
510(k) Number K960742
Device Name TYMPANOSTOMY VENTILATION TUBE
Applicant
ADVANCED MICROBOTICS CORP.
2611 S.W. 3RD. AVE., SUITE 200
PORTLAND,  OR  97201
Applicant Contact ANTHONY W HUMPAGE
Correspondent
ADVANCED MICROBOTICS CORP.
2611 S.W. 3RD. AVE., SUITE 200
PORTLAND,  OR  97201
Correspondent Contact ANTHONY W HUMPAGE
Regulation Number874.3880
Classification Product Code
ETD  
Date Received02/23/1996
Decision Date 04/03/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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