FDA 510(k) Applications Submitted by GARY CURTIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000032 | 01/05/2000 | LEVEEN NEEDLE ELECTRODE | RADIOTHERAPEUTICS CORP. |
| K000241 | 01/27/2000 | RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR | RADIOTHERAPEUTICS CORP. |
| K011220 | 04/20/2001 | LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE | RADIOTHERAPEUTICS CORP. |
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