FDA 510(k) Applications Submitted by JEFFERY W COBB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020778 | 03/11/2002 | GYRUS ENT SOMNOPLASTY TISSUE COAGULATING ELECTRODE, MODEL 2420 | GYRUS ENT L.L.C. |
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