FDA 510(k) Applications Submitted by NEBL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971359 | 04/11/1997 | RESTORE (A.K.A. CAPSURE) | NEBL, INC. |
| K983164 | 09/10/1998 | RESTORE (AKA RE/STOR) | NEBL, INC. |
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