FDA 510(k) Applications Submitted by SUZANNE DEW
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K083684 | 12/12/2008 | ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX | MANUFACTURING & RESEARCH, INC. |
| K083685 | 12/12/2008 | ENDOVIVE LOW PROFILE REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX, 8283, 8284, 8285 | MRI MANUFACTURING AND RESEARCH, INC. |
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