FDA 510(k) Applications Submitted by JUDI WEISSINGER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K123386 | 11/02/2012 | PERIOTYPE X-PERT | CLINICAL HOUSE EUROPE GMBH |
| K143758 | 12/31/2014 | PerioType Rapid | CLINICAL HOUSE EUROPE GMBH |
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