FDA 510(k) Applications Submitted by JOHNSON & JOHNSON PRODUTOS PROFISSIONAIS LTDA.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080040 | 01/07/2008 | ORTHO ALL-FLEX DIAPHRAGM | JOHNSON & JOHNSON PRODUTOS PROFISSIONAIS LTDA. |
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