Medical device makerLabelled 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 15, 2026, FDA's public records list KT Medical, Inc. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jul 21, 1980: SINVISION LINEAR ARRAY REAL TIME.
| Jul 21, 1980 | SINVISION LINEAR ARRAY REAL TIMEK800653 · DXK | 510(k) clearances |
| May 14, 1980 | MODEL E03 ECHO-OPTHALMOSCOPEK800652 · IYO | 510(k) clearances |
| May 2, 1980 | 4200 ME ECHOENCEPHALOGRAPHK800101 · IYO | 510(k) clearances |
| Apr 8, 1980 | COMBISON COMPUTERK800092 · DQK | 510(k) clearances |
| Feb 21, 1980 | 7200 MA ECHO-OPHTHALMOSCOPEK800100 · IYO | 510(k) clearances |
| Feb 21, 1980 | INTRACULA IIK800099 · IYO | 510(k) clearances |
| Feb 11, 1980 | COMBISON 200 & COMBISON 202K800094 · IYO | 510(k) clearances |
| Feb 11, 1980 | MGD-3K800095 · KNG | 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
