FDA 510(k) Applications Submitted by NEUROTHERM, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111576 | 06/06/2011 | NT 2000 LESIONING GENERATOR | NEUROTHERM, INC. |
| K052878 | 10/12/2005 | NT-1000 | NEUROTHERM, INC. |
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