FDA 510(k) Applications Submitted by DEBORAH MOORE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K964760 | 11/27/1996 | DORNIER MEDILAS FIBER TOME LASER | DORNIER MEDTECH AMERICA, INC. |
| K003206 | 10/13/2000 | GLIASITE RADIATION THERAPY SYSTEM (RTS), MODEL 1020,1030,1040,8150,9005 | PROXIMA THERAPEUTICS, INC. |
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