FDA 510(k) Applications Submitted by JOSEPH CURTIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011988 | 06/26/2001 | SURGICAL LIGHTSTIC 180, MODEL 180 L, MODEL 180 C | CARDIOFOCUS, INC. |
| K013901 | 11/26/2001 | MALLEABLE SURGICAL LIGHTSTIC 180, MODEL 180 (1CM-9CM) | CARDIOFOCUS, INC. |
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