FDA 510(k) Applications Submitted by Buffalo Filter, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171139 | 04/18/2017 | LaparoLight Veress Needle | Buffalo Filter, LLC |
| K150569 | 03/06/2015 | LaparoVue | Buffalo Filter, LLC |
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