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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Endoscopic Cytology Brush
510(k) Number K860997
Device Name GASTROINTESTINAL CYTOLOGY BRUSH
Applicant
Endovations
895 Poplar Church Rd.
Camp Hill,  PA  17011
Applicant Contact LESTER J LIFTON
Correspondent
Endovations
895 Poplar Church Rd.
Camp Hill,  PA  17011
Correspondent Contact LESTER J LIFTON
Regulation Number876.1500
Classification Product Code
FDX  
Date Received03/18/1986
Decision Date 05/02/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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