FDA 510(k) Applications Submitted by TE ME NA SAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060186 | 01/24/2006 | POLYPLEX STIMULATING CATHETER SYSTEM | TE ME NA SAS |
| K080603 | 03/03/2008 | HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED | TE ME NA SAS |
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