FDA 510(k) Applications Submitted by GUIDO BONAPACE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080132	01/18/2008	THD DISPOSABLE ANOSCOPE/PROCTOSCOPE	THD SPA
K120318	02/02/2012	VIVI ERGON-X HF	VIVI S.R.L.
K070494	02/20/2007	EPI-C PLUS	ESPANSIONE MARKETING SPA
K121135	04/13/2012	THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPE	THD SPA
K091390	05/11/2009	HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2	HDC S.R.L.
K091490	05/20/2009	FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPES	THD SPA
K071851	07/05/2007	HDC STERILE SPIDER SCREW	HDC S.R.L.
K092734	09/04/2009	E-LIGHT LINE	ESPANSIONE MARKETING S.P.A
K132772	09/05/2013	LUBRIGYN CREAM	UNIDERM FARMACEUTICI SRL
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
K124064	12/31/2012	YOUNG AGAIN	ESPANSIONE MARKETING SPA