FDA 510(k) Applications Submitted by SOPRO

FDA 510(k) Number Submission Date Device Name Applicant
K020270 01/28/2002 SOPRO 367D 3CCD FULL DIGITAL ENDOSCOPY CAMERA SOPRO
K000422 02/09/2000 S57D DIGITAL OPERATING ROOM CAMERA SOPRO
K000423 02/09/2000 S52D DIGITAL VIDEO LAPAROSCOPE SOPRO
K000424 02/09/2000 S51D DIGITAL ENDOSCOPY CAMERA SOPRO
K020915 03/21/2002 SOPRO LIGHT SOURCES AND ACCESSORIES SOPRO
K990948 03/22/1999 S575 INTRAORAL DOCKING DENTAL CAMERA SOPRO
K031593 05/21/2003 SOPRO 61D SOPRO
K972540 07/07/1997 S-357 VIDEO IMAGING SYSTEM SOPRO
K012505 08/03/2001 SOPRO595 INTRA ORAL CAMERA SOPRO
K013090 09/17/2001 SOPRO 67D OPERATING ROOM CAMERA SOPRO
K973794 10/06/1997 S-57 VIDEO IMAGING SYSTEM SOPRO
K973795 10/06/1997 S-52 ELECTRONIC VIDEO LAPAROSCOPE SOPRO
K973796 10/06/1997 S-41 &41S VIDEO IMAGING SYSTEM SOPRO
K973798 10/06/1997 S-357 VIDEO IMAGING SYSTEM SOPRO
K983625 10/15/1998 S555 INTRAORAL DENTAL CAMERA SOPRO
K121685 06/07/2012 SOPROCARE SOPRO
K092329 08/04/2009 SOPIX 2 SOPRO
K092583 08/21/2009 SOPROLIFE SOPRO
K082796 09/23/2008 SOPRO 184 CAMERA SOPRO
K103813 12/29/2010 SOPRO 281 SOPRO
K070102 01/10/2007 SOPRO 162 CAMERA SOPRO
K080122 01/17/2008 SOPRO 670 ARTHROSCOPIC PUMP SOPRO
K070783 03/21/2007 SOPRO MODEL 640 LAPAROSCOPIC INSUFFLATOR SOPRO
K072912 10/12/2007 SOPRO 225 DUAL HALOGEN LIGHT SOURCE SOPRO


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