LASERSCAN LSX EXCIMER LASER SYSTEM

Excimer Laser System

FDA Premarket Approval P980008 S008

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval to increase the pulse rate of the laser from 100 to 200 hz.

DeviceLASERSCAN LSX EXCIMER LASER SYSTEM
Classification NameExcimer Laser System
Generic NameExcimer Laser System
ApplicantLASERSIGHT TECHNOLOGIES, INC.
Date Received2001-10-05
Decision Date2001-10-25
PMAP980008
SupplementS008
Product CodeLZS
Advisory CommitteeOphthalmic
Supplement TypeReal-time Process
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address LASERSIGHT TECHNOLOGIES, INC. 6903 University Blvd., winter Park, FL 32792

Supplemental Filings

Supplement NumberDateSupplement Type
P980008Original Filing
S012 2002-10-31 Real-time Process
S011
S010
S009 2001-10-26 Special (immediate Track)
S008 2001-10-05 Real-time Process
S007
S006
S005 2000-12-19 Panel Track
S004
S003 2000-07-20 Real-time Process
S002 2000-07-13 Normal 180 Day Track
S001

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.