FDA 510(k) Applications Submitted by JAMES BOYD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181005 | 04/16/2018 | ClenchGuard | Boyd Research, Inc. |
| K211158 | 04/19/2021 | NTI ClenchGuard | Boyd Research, Inc. |
| K041184 | 05/06/2004 | NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION | NTI-TSS, INC. |
| K032410 | 08/04/2003 | SNORENTI | JAMES P BOYD |
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