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 Kontron Instruments Ltd. with 58 510(k) clearances. The most recent is a 510(k) clearance dated Sep 24, 1997: KONTRON KOLORMON PLUS ECG WITH RESPIRATION MODULE.
| Date | Record | Source |
|---|---|---|
| Sep 24, 1997 | KONTRON KOLORMON PLUS ECG WITH RESPIRATION MODULEK971038 · DPS | 510(k) clearances |
| Dec 15, 1993 | MODIFICATIONS TO INTRA-AORTIC BALLOONSK932268 · DSP | 510(k) clearances |
| Sep 27, 1993 | MODIFICATION OF INTRA-AORTIC BALLOON CATHETERSK925248 · DSP | 510(k) clearances |
| Mar 8, 1993 | INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATIONK923603 · DYB | 510(k) clearances |
| Jun 19, 1991 | KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT IIK905313 · DSP | 510(k) clearances |
| Jan 15, 1991 | 9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)K903344 · DSP | 510(k) clearances |
| Dec 3, 1990 | KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEMK896437 · DPT | 510(k) clearances |
| Sep 14, 1990 | 9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOONK892222 · DSP | 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
