FDA 510(k) Applications Submitted by NEOMEDIX CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K024304 | 12/24/2002 | MICROSURGICAL BIPOLAR HANDPIECE | NEOMEDIX CORP. |
| K040239 | 02/02/2004 | SUPRAFLOW CONSOLE | NEOMEDIX CORP. |
| K040584 | 03/05/2004 | NMX-1000 | NEOMEDIX CORP. |
| K061258 | 05/05/2006 | TRABECTOME HIGH FREQUENCY GENERATOR/LP | NEOMEDIX CORP. |
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