FDA 510(k) Applications Submitted by EDDIE MONROE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990173 | 01/19/1999 | PATHFINDER II ANGIOGRAPHIC CATHETER | MAXXIM MEDICAL |
| K984189 | 11/23/1998 | ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER | MAXXIM MEDICAL |
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