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 Oxford Medilog with 48 510(k) clearances. The most recent is a 510(k) clearance dated Jan 5, 1994: MODEL MEDILOG RAPIDE.
| Jan 5, 1994 | MODEL MEDILOG RAPIDEK923737 · BZQ | 510(k) clearances |
| Aug 18, 1992 | MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)K920295 · DQK | 510(k) clearances |
| Jan 9, 1992 | MODEL SONICAID AXISK912890 · HGM | 510(k) clearances |
| Dec 31, 1991 | SONICAID TEAMK912639 · HGM | 510(k) clearances |
| Apr 10, 1991 | MENTOR EEG SYSTEMK904763 · GWQ | 510(k) clearances |
| Feb 5, 1991 | SONICAID MODEL MERIDIAN 800K902690 · HGM | 510(k) clearances |
| Jul 9, 1990 | SONICAID MODEL VASOFLO 4K895909 · MAA | 510(k) clearances |
| Jan 18, 1990 | MEDILOG OPTIMAK896535 · DSK | 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
