Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 Oakfield Instruments Ltd with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 6, 1997: FLEXILOG LS.
| Date | Record | Source |
|---|---|---|
| Aug 6, 1997 | FLEXILOG LSK964804 · KLA | 510(k) clearances |
| Mar 4, 1997 | FLEXILOG 3000K964589 · KLA | 510(k) clearances |
| Nov 4, 1996 | FLEXILOG LS 13921K961895 · KLA | 510(k) clearances |
| Jun 13, 1995 | FLEXILOG 2000K945069 · FFT | 510(k) clearances |
| Mar 30, 1992 | MEDISCINTK920115 · IZD | 510(k) clearances |
| Aug 28, 1990 | CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)K902460 · IZD | 510(k) clearances |
| May 4, 1990 | FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEMK896288 · FFT | 510(k) clearances |
| Oct 17, 1989 | SOURCERERK894902 · JJJ | 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
