FDA 510(k) Applications Submitted by COMPEX TECHNOLOGIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050046 | 01/10/2005 | REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S | COMPEX TECHNOLOGIES, INC. |
| K061516 | 06/01/2006 | STAODYN MAX PRESET, MODEL 4470 | COMPEX TECHNOLOGIES, INC. |
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