Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 8 companies' records, each linked to the record.
As of Nov 13, 2026, FDA's public records list Smiths Group and its 8 subsidiaries with 101 510(k) clearances. The most recent is a 510(k) clearance dated Apr 29, 2025: Qitexio® 4-Way Stopcock (QIT014).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Smiths Group and its 8 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Apr 29, 2025 | Qitexio® 4-Way Stopcock (QIT014)K242255 · FMG | 510(k) clearances |
| Mar 14, 2022 | QitexioK203738 · FMF | 510(k) clearances |
| Oct 28, 2014 | EQUATOR CONVECTIVE WARMER, SNUGGLE WARM ADULT FULL BODY CONVECTIVE WARMING BLANKET, SNUGGLE WARM PEDIATRICFULL BODYK141686 · DWJ | 510(k) clearances |
| May 1, 2009 | BCI WW1030 PULSE OXIMETERK083557 · DQA | 510(k) clearances |
| Apr 28, 2009 | BCI WW1021 PC APPLICATIONK090205 · DQA | 510(k) clearances |
| Apr 15, 2009 | BCI WW1000 PULSE OXIMETER, MODEL WW1000K083787 · DQA | 510(k) clearances |
| Apr 9, 2009 | BCI WW1020 PULSE OXIMETER, MODEL WW1020K083705 · DQA | 510(k) clearances |
| Jul 9, 2007 | BCI AUTOCON 3304 DIGITAL PULSE OXIMETERK070732 · DQA | 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
