FDA 510(k) Applications Submitted by POINTDX, INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030457 | 02/11/2003 | REX, VERSION 3.0 | POINTDX, INC |
| K021099 | 04/04/2002 | REX, VERSION 1.0 | POINTDX, INC |
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