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FDA 510(k) Applications for Medical Device Product Code "LRB"
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| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K974219 | FINETONE HEARING INSTRUMENTS | FACEPLATE ASSEMBLY | 02/20/1998 |
| K961593 | SEGI HEARING AID CO. | INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDS | 11/07/1996 |