FDA 510(k) Applications Submitted by JOHN WESTERMEIER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K012308 | 07/23/2001 | KAVO QUATTROCARE | KAVO AMERICA |
| K002708 | 08/30/2000 | KAVO CORUND HANDPIECE 2013 | KAVO AMERICA |
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