Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Thermo Fisher ScientificLabelled by claude-sonnet-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 Kone Instruments, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Sep 11, 1987: 'MICROLYTE 4/5'.
| Date | Record | Source |
|---|---|---|
| Sep 11, 1987 | 'MICROLYTE 4/5'K873345 · JFP | 510(k) clearances |
| Mar 13, 1987 | PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZERK870777 · JJF | 510(k) clearances |
| Dec 22, 1986 | M700 STRESS MONITORK863466 · DRT | 510(k) clearances |
| Aug 6, 1986 | SIGNA II RESTING ECG ELECTRODEK862655 · DRX | 510(k) clearances |
| Apr 23, 1986 | MODEL E 600 ELECTROCARDIOGRAPHK860767 · DSI | 510(k) clearances |
| Oct 11, 1985 | MEDIC 4K853354 · LDD | 510(k) clearances |
| Apr 4, 1984 | PROGRESS SELECTIVE DHEMISTRY ANALYZK840200 · JJF | 510(k) clearances |
| Mar 24, 1983 | PATIENT MONITOR 575K830433 · DRT | 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
