FDA 510(k) Applications Submitted by STEVEN HARTMAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071378 | 05/17/2007 | MODIFICATION TO EMPOWER CT/CTA INJECTOR SYSTEM, MODELS 9800/9900 PRODUCT SERIES | E-Z-EM, INC. |
| K031571 | 05/20/2003 | EMPOWERCTA INJECTOR SYSTEM, MODELS 9930 & 9910 & 9825 | E-Z-EM, INC. |
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