FDA 510(k) Applications Submitted by KLASS BESSELING
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062834 | 09/21/2006 | OSTEON, MODELS GBG0305, GBG0510, GBG1020, GBG2030, GBG3040, GBG4050 | GENOSS CO., LTD. |
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