FDA 510(k) Applications Submitted by RLN SYSTEMS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K003745 | 12/04/2000 | LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET | RLN SYSTEMS, INC. |
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