FDA 510(k) Application Details - K182231

Device Classification Name Endoscopic Cytology Brush

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510(K) Number K182231
Device Name Endoscopic Cytology Brush
Applicant Cook Incorporated
750 Daniels Way
Bloomington, IN 47404 US
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Contact Thomas Palmer
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Regulation Number 876.1500

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Classification Product Code FDX
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Date Received 08/17/2018
Decision Date 05/01/2019
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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