FDA 510(k) Applications Submitted by GREGORY W BOWMAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K973876 | 10/10/1997 | PROPHYFLEX 2, MODEL 2012 | KAVO AMERICA |
| K003787 | 12/08/2000 | NEWTOM QR-DVT 9000 | APERIO SERVICES, LLC |
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