FDA 510(k) Applications Submitted by NEURO-BIOMETRIX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K973740 | 10/01/1997 | ROUND WINDOW E-CATH | NEURO-BIOMETRIX, INC. |
| K965115 | 12/20/1996 | ROUND WINDOW CATH | NEURO-BIOMETRIX, INC. |
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