FDA 510(k) Applications Submitted by RICHARD W POORE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960508 | 02/05/1996 | PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25 | THE PROMETHEUS GROUP |
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