FDA 510(k) Applications Submitted by TONYA WEIGEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K982657 | 07/30/1998 | AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100 | MICROVENA CORP. |
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