FDA 510(k) Applications Submitted by KAVO AMERICA CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K042394 | 09/02/2004 | DIAGNODENT PERIO TIP (ACCESSORY) | KAVO AMERICA CORPORATION |
| K033221 | 10/03/2003 | KAVO EVEREST ZH-BLANK | KAVO AMERICA CORPORATION |
| K042872 | 10/18/2004 | RONDOFLEX PLUS 360 | KAVO AMERICA CORPORATION |
| K050744 | 03/22/2005 | KAVO ERGOCOM/ERGOCAM | KAVO AMERICA CORPORATION |
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