FDA 510(k) Applications Submitted by INTRA LASE CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060372 | 02/13/2006 | INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3 | INTRA LASE CORP. |
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