Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of SiemensLabelled 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 Acuson with 37 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 2002: KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM.
| Date | Record | Source |
|---|---|---|
| Nov 22, 2002 | KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEMK023772 · LLZ | 510(k) clearances |
| Oct 3, 2002 | CSV12 SOFTWARE VIEWERK022896 · LLZ | 510(k) clearances |
| Aug 13, 2002 | SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEMK022567 · IYN | 510(k) clearances |
| Jul 9, 2002 | CYPRESS ULTRASOUND SYSTEMK021497 · IYN | 510(k) clearances |
| Jun 27, 2001 | CYPRESS SYSTEMK010950 · IYO | 510(k) clearances |
| Dec 1, 2000 | 3D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSINGK002807 · IYO | 510(k) clearances |
| Dec 15, 1999 | ACUNAV DIAGNOSTIC ULTRASOUND CATHETERK992631 · DQO | 510(k) clearances |
| Oct 18, 1999 | FETAL ASSESSMENT CAPK992580 · IYO | 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
