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 Wright Linear Pump with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 2007: WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMS.
| Date | Record | Source |
|---|---|---|
| May 22, 2007 | WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMSK071040 · JOW | 510(k) clearances |
| Nov 6, 1996 | WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITEK961797 · JOW | 510(k) clearances |
| Nov 6, 1996 | WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIALK961292 · JOW | 510(k) clearances |
| Nov 6, 1996 | WLP SINGLE-SEGMENT VERSION WLP SOLO VIIK961891 · JOW | 510(k) clearances |
| Nov 21, 1988 | WRIGHT GRADIENT PRESSURE SUPPORT STOCKINGSK883186 · DWL | 510(k) clearances |
| May 25, 1983 | LINEAR PUMP #4370975K830577 · JOW | 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
