FDA 510(k) Applications Submitted by LUMALITE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K002566 | 08/17/2000 | LUMALITE CURE LIGHT, MODEL 2100 | LUMALITE, INC. |
| K021083 | 04/03/2002 | VERACAM | LUMALITE, INC. |
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