FDA 510(k) Applications Submitted by MEDICAL DEVICES/PADPRO, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061606 | 06/09/2006 | DEFIBRILLATOR CABLE TESTER, MODEL DT2200 | MEDICAL DEVICES/PADPRO, INC. |
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