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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 K981966
Device Name NOSEBLEED NOSECLIP
Applicant
MICHAEL M. KNOTT, M.D.
355 ROSE PINE COURT
PO BOX 5577
TAHOE CITY,  CA  96145 -5577
Applicant Contact MICHAEL M KNOTT
Correspondent
MICHAEL M. KNOTT, M.D.
355 ROSE PINE COURT
PO BOX 5577
TAHOE CITY,  CA  96145 -5577
Correspondent Contact MICHAEL M KNOTT
Regulation Number874.4100
Classification Product Code
EMX  
Date Received06/04/1998
Decision Date 08/14/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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