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 13, 2026, FDA's public records list Ketronic with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jun 12, 1985: MFE CARDIAC STRESS SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jun 12, 1985 | MFE CARDIAC STRESS SYSTEMK850868 · | 510(k) clearances |
| Jun 12, 1985 | MEDIFETTE ERGOMETERK850870 · | 510(k) clearances |
| Jun 12, 1985 | HILO TABLES, TYPE CH-4, CH-8, FW-6, FW-5, FW-2, ALK850873 · INO | 510(k) clearances |
| Jun 12, 1985 | MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFORK850877 · ILK | 510(k) clearances |
| Jun 12, 1985 | MFE COUCH ERGOMETERK850869 · ISD | 510(k) clearances |
| Jun 6, 1985 | PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STIK850872 · | 510(k) clearances |
| Jun 5, 1985 | TREDBAND TYPE I, IT, II & III - TREADMILLSK850871 · BXB | 510(k) clearances |
| May 16, 1985 | LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIRK850876 · ITI | 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
