FDA 510(k) Applications Submitted by JODI LOCHER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963367 | 08/27/1996 | RMS K-WIRE | RMS DIV. |
| K954205 | 09/07/1995 | THE AMPLATZ THROMBECTOMY DEVICE | MICROVENA CORP. |
| K954642 | 10/10/1995 | HYDRO-SELECT GUIDEWIRE | MICROVENA CORP. |
| K955304 | 11/20/1995 | CRICKET | MICROVENA CORP. |
| K993248 | 09/28/1999 | AMPLATZER SIZING BALLOON | AGA MEDICAL CORP. |
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