Topcon Medical Laser Systems, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Topcon Medical Laser Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 6 cleared submissions from 2005 to 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Topcon Medical Laser Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Topcon Medical Laser Systems, Inc.
6 devices
Cleared
May 25, 2018
PSLT with PASCAL Synthesis, PSLT with PASCAL Synthesis TwinStar
Ophthalmic
100d
Cleared
Nov 27, 2017
PSLT for PASCAL Streamline
Ophthalmic
189d
Cleared
May 15, 2013
PASCAL SYNTHESIS (532NM/577NM) OPTHALMIC LASER
Ophthalmic
177d
Cleared
Aug 11, 2011
PASCAL STREAMLINE 577 (WITH ACCESSORIES)
Ophthalmic
113d
Cleared
Sep 25, 2009
PASCAL STREAMLINE PHOTOCOAGULATOR
Ophthalmic
30d
Cleared
Mar 03, 2005
PASCAL PHOTOCOAGULATOR, PRODUCT-PASCAL-01
General & Plastic Surgery
76d