ILT SURGICAL LASER— 510(k) K954460

Substantially Equivalent

Ion Laser Technology

FDA 510(k) clearance K954460 for ILT SURGICAL LASER, Substantially Equivalent on 1995-12-18. Applicant: Ion Laser Technology. Device class: 2.

Clearance details

Applicant
Ion Laser Technology
Product code
Code GEX
Device class
Class 2
Regulation
21 CFR 878.4810
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Salt Lake City, UT, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code GEX

view all

More clearances from Ion Laser Technology

view all

Adverse events under product code GEX

product code GEX
Death
33
Injury
3,045
Malfunction
12,903
Other
25
Total
16,006

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.