Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Upstream Peripheral Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 1, 2022: GoBack Crossing Catheter.
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 1, 2022 | GoBack Crossing CatheterK211802 · PDU | 510(k) clearances |
| May 23, 2019 | Upstream GoBack Crossing CatheterK182937 · DQY | 510(k) clearances |
| May 25, 2012 | UPSTREAM GR CATHETERK120964 · DQY | 510(k) clearances |
| Mar 21, 2012 | UPSTREAM NEEDLE HOLDER, UPSTREAM NEEDLE HOLDER WITH SHUT-OFF CONNECTORK112887 · DYB | 510(k) clearances |
| Feb 23, 2012 | UPSTREAM SUPPORT CATHETERK112886 · DQY | 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
