Tinnitus Treatment Centers, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K982451 | TTCGHI-T AND TTCTN3-T-T | KLW | 1999-05-07 | View |
| 510(k) | K982432 | PILLOW MASKER, C2007M, C2008M,CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5- | KLW | 1999-01-25 | View |
No matching devices.
Advertisement