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.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Interson Corporation with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 2023: Interson USB Ultrasound System.
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 |
|---|---|---|
| Dec 22, 2023 | Interson USB Ultrasound SystemK233734 · IYN | 510(k) clearances |
| Apr 13, 2017 | Interson USB Ultrasound SystemK163443 · IYN | 510(k) clearances |
| Dec 20, 1991 | INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYSTK911116 · ITX | 510(k) clearances |
| Dec 17, 1991 | INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYSTK911113 · ITX | 510(k) clearances |
| Dec 17, 1991 | INTERSON TRANSRECTAL PROBE/ATL ULTRASOUND SYSTEMK911115 · ITX | 510(k) clearances |
| Dec 17, 1991 | INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYSTK911117 · ITX | 510(k) clearances |
| Nov 19, 1991 | INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEMK911114 · ITX | 510(k) clearances |
| Sep 27, 1991 | INTERSON DISPOSABLE BIOPSY NEEDLEK911464 · 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
