FDA 510(k) Applications Submitted by LISA HENRY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080171 | 01/24/2008 | SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012 | SANARUS MEDICAL, INC. |
| K073533 | 12/17/2007 | SANARUS V2 TREATMENT SYSTEM | SANARUS MEDICAL, INC. |
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