FDA 510(k) Applications Submitted by VENOWAVE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K073028 | 10/26/2007 | VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30 | VENOWAVE, INC. |
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