FDA 510(k) Applications Submitted by JOSEPH FOREHAND
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990060 | 01/08/1999 | MACH 7 | KREATIV, INC. |
| K992102 | 06/21/1999 | LUMA LIGHT 2000 CURE LIGHT | LUMA LITE, INC, |
| K002566 | 08/17/2000 | LUMALITE CURE LIGHT, MODEL 2100 | LUMALITE, INC. |
| K983227 | 09/15/1998 | POWER BLOCK | KREATIV, INC. |
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