FDA 510(k) Applications Submitted by JORDAN HARTONG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K051068 | 04/26/2005 | ZUTRON COLONOSCOPE STIFFENING DEVICE | ZUTRON MEDICAL |
| K093718 | 12/02/2009 | ZUTRON MEDICAL ENDOSCOPE LEAK TESTER MODEL ZUTR-10003 | ZUTRON MEDICAL LLC |
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