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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Balloon, Epistaxis
510(k) Number K900583
Device Name MODIFIED BIVONA EPISTAXIS CATHETER
Applicant
Bivona Medical Technologies
5700 W. 23rd Ave.
Gary,  IN  46406
Applicant Contact HARRY M KAUFMAN
Correspondent
Bivona Medical Technologies
5700 W. 23rd Ave.
Gary,  IN  46406
Correspondent Contact HARRY M KAUFMAN
Regulation Number874.4100
Classification Product Code
EMX  
Date Received02/07/1990
Decision Date 08/09/1990
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
Predetermined Change
Control Plan Authorized		 No
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