FDA 510(k) Applications Submitted by PETER SULLIVAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030039 | 01/06/2003 | PATHWAY STM-10 PELVIC FLOOR STIMULATOR | THE PROMETHEUS GROUP |
| K960761 | 02/26/1996 | PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20 | THE PROMETHEUS GROUP |
| K973537 | 09/18/1997 | PATHWAY ELECTROMYOGRAPH | THE PROMETHEUS GROUP |
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