Buffalo Filter, LLC is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Buffalo Filter, LLC - FDA 510(k) Cleared Devices
Recent clearances: LaparoLight Veress Needle, LaparoVue
2
Total
2
Cleared
0
Denied
Buffalo Filter, LLC has 2 FDA 510(k) cleared medical devices. Based in Lancaster, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Buffalo Filter, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Third Party Review Group, LLC and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Buffalo Filter, LLC
2 devices