FDA 510(k) Applications Submitted by A. ROBERT DEPALMA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032329 | 07/29/2003 | SA 9900 PLUS DIAGNOSTIC ULTRASOUND SYSTEM | MEDISON AMERICA, INC. |
| K013627 | 11/05/2001 | SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM | MEDISON AMERICA, INC. |
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