FDA 510(k) Applications Submitted by NEUROLUMEN, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142025 | 07/25/2014 | NEUROLUMEN PN-1000 | NEUROLUMEN, LLC |
| K082223 | 08/06/2008 | NEUTROLUMENPN SYSTEM, MODEL 1000 | NEUROLUMEN, LLC |
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