Intra Lase Corp.
Intra Lase Corp. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2008.
Top product codes for Intra Lase Corp.
Recent clearances by Intra Lase Corp.
- K073404 — IFS LASER SYSTEM
- K063682 — INTRALASE FUSION LASER
- K060372 — INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3
- K041893 — INTRALASE FS LASER
- K031960 — INTRALASE FS LASER
- K013941 — PULSION FS LASER KERATOME
- K002890 — INTRALASE 600C LASER KERATOME
- K001211 — MODIFICATION TO INTRALASE 600C LASER KERATOME
- K993153 — INTRALASE 600C LASER KERATOME
Data sourced from openFDA. This site is unofficial and independent of the FDA.