FDA 510(k) Applications Submitted by THD SpA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K193512	12/18/2019	THD Procto Software System	THD SpA
K161785	06/29/2016	THD ANOPRESS	THD SPA
K080132	01/18/2008	THD DISPOSABLE ANOSCOPE/PROCTOSCOPE	THD SPA
K121135	04/13/2012	THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPE	THD SPA
K091490	05/20/2009	FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPES	THD SPA
K093497	11/12/2009	THD BANDY	THD SPA
K133687	12/02/2013	THD N-ANO ANOSCOPE	THD SPA
K103647	12/13/2010	THD DISPOSABLE ANOSCOPES, PROCTOSCOPES AND RECTOSCOPES	THD SPA
K090009	01/02/2009	THD SLIDE ONE	THD SPA
K081429	05/21/2008	THD SLIDE	THD SPA
K180135	01/17/2018	THD Anopress with THD SensyProbe	THD SpA
K211623	05/26/2021	THD Procto Software System	THD SpA
K141657	06/20/2014	THD REVOLUTION	THD SPA