FDA 510(k) Applications Submitted by REGINA YEH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020089 | 01/10/2002 | MAHURKAR TRIPLE LUMEN CATHETER, 12 FR | THE KENDALL COMPANY |
| K000087 | 01/12/2000 | MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR | THE KENDAL CO. |
| K030209 | 01/21/2003 | MAHURKAR OPLUS CATHETER, MODEL 13.5 FR | THE KENDALL COMPANY |
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