FDA 510(k) Applications Submitted by TINNITUS CONTROL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061111 | 04/21/2006 | TINNITUS PHASE-OUT | TINNITUS CONTROL, INC. |
| K031624 | 05/23/2003 | TINNITUS RX | TINNITUS CONTROL, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact