FDA 510(k) Applications for Medical Device Product Code "BTG"
(Brush, Biopsy, Bronchoscope (Non-Rigid))

FDA 510(k) Number Applicant Device Name Decision Date
K780872 COOPERVISION, INC. CYTOLOGY BRUSH 09/07/1978
K130357 COVIDIEN LLC SUPERDIMENSION TRIPLE-NEEDLE CYTOLOGY BRUSH 11/06/2013
K820771 MILL-ROSE LABORATORY MICROBIOLOGY SPECIMEN BRUSH 05/03/1982


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