FDA 510(k) Applications Submitted by METALOR TECHNOLOGIES USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K013505 | 10/22/2001 | AUROFLUID PLUS | METALOR TECHNOLOGIES USA |
| K013506 | 10/22/2001 | YELLOW SPECIAL | METALOR TECHNOLOGIES USA |
| K020062 | 01/08/2002 | XERAFIT | METALOR TECHNOLOGIES USA |
| K013769 | 11/13/2001 | V-GNATHOS SUPRA | METALOR TECHNOLOGIES USA |
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