Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Clearflow with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 2, 2021: PleuraFlow System with FlowGlide.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Mar 2, 2021 | PleuraFlow System with FlowGlideK203394 · OTK | 510(k) clearances |
| Jul 26, 2019 | The ZIP Accessory Shuttle for PleuraFlow SystemK191733 · OTK | 510(k) clearances |
| Aug 14, 2018 | PleuraFlow System with FlowGlide Extra Drainage LengthK182067 · OTK | 510(k) clearances |
| Nov 30, 2016 | PleuraFlow System with FlowGlideK163139 · OTK | 510(k) clearances |
| Jan 20, 2016 | PleuraFlow SystemK153681 · OTK | 510(k) clearances |
| Jun 2, 2015 | PleuraFlow SystemK150042 · OTK | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
