FDA 510(k) Applications for Medical Device Product Code "LRB"
|
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 |