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 Syntermed with 14 510(k) clearances. The most recent is a 510(k) clearance dated Mar 30, 2023: Emory Cardiac Toolbox 4.3.
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 30, 2023 | Emory Cardiac Toolbox 4.3K223422 · KPS | 510(k) clearances |
| Aug 16, 2018 | NeuroQ 3.8K180077 · KPS | 510(k) clearances |
| Jun 14, 2013 | EMORY CARDIAC TOOLBOX 3.2K130902 · KPS | 510(k) clearances |
| May 17, 2013 | NEUROQ 3.6K130451 · KPS | 510(k) clearances |
| Feb 22, 2013 | EMORY CARDIAC TOOLBOX 4.0K123646 · KPS | 510(k) clearances |
| Mar 14, 2008 | QUANTITATIVE NEUROQ 3.0K072307 · KPS | 510(k) clearances |
| Jul 26, 2007 | SYSTEM, TOMOGRAPHY, COMPUTED EMISSIONK071503 · KPS | 510(k) clearances |
| Mar 2, 2007 | SYNTERMED LIVEK070089 · LLZ | 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
