FDA 510(k) Applications Submitted by PROSURG, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K120766 03/13/2012 ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION) PROSURG, INC.
K060326 02/09/2006 LASERTX - DIODE LASER & DELIVERY SYSTEM PROSURG, INC.
K050488 02/25/2005 TURBT-RF ELECTRODES AND ELECTROSURGICAL DEVICES PROSURG, INC.
K030631 02/28/2003 ZIPPERE - BIOABSORBABLE/NON-ABSORBABLE POLYMER SLING & SURGICAL MESH PROSURG, INC.
K070737 03/16/2007 XSORB BIOABSORBABLE CRANIOFACIAL BONE FIXATION SYSTEM & ACCESSORIES PROSURG, INC.
K071138 03/16/2007 CRANIOCLAMP BIOABSORBABLE CRANIAL BONE FLAP FIXATION SYSTEM PROSURG, INC.
K070846 03/28/2007 MINISLING ADJUSTABLE POLYMER SLING & SURGICAL MESH WITH SELF-ANCHORING SYSTEM PROSURG, INC.
K072528 09/07/2007 ADJUSTABLE BONE PLATES BIOABSORBABLE, SELF COMPRESSION BONE FIXATION SYSTEM & ACCESSORIES PROSURG, INC.
K023051 09/13/2002 INTRAUTERINE DELIVERY SYSTEM - INJECTOR PROSURG, INC.
K152619 09/14/2015 Neoscope 3D - 3D Digital Video Endoscopic System (Rigid/Flexible) PROSURG, INC.
K023257 09/30/2002 ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX PROSURG, INC.
K042780 10/06/2004 NEOSCOPE - ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM PROSURG, INC.
K000124 01/18/2000 SENSATION -VACUUM ASSIST DEVICES PROSURG, INC.
K001576 05/22/2000 EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY PROSURG, INC.


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