FDA 510(k) Applications Submitted by JIM GIBSON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010292 | 01/31/2001 | DRX 2000 | AXIOM WORLDWIDE, INC. |
| K060735 | 03/20/2006 | DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM | AXIOM WORLDWIDE, INC. |
| K022602 | 08/06/2002 | DRX3000 | AXIOM USA. INC |
| K023160 | 09/23/2002 | DRX5000 | AXIOM USA. INC |
| K033015 | 09/26/2003 | AXIOM BIOLASER LLLT SERIES-3 | AXIOM USA. INC |
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