Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 OEC-Diasonics, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 21, 1993: 9600 FLUOROSCOPIC IMAGING SYSTEM.
| Jan 21, 1993 | 9600 FLUOROSCOPIC IMAGING SYSTEMK926056 · OXO | 510(k) clearances |
| Jan 4, 1993 | EP 3000K924879 · JAA | 510(k) clearances |
| Jan 10, 1992 | UROVIEW 2000, MODIFICATIONK914446 · JAA | 510(k) clearances |
| Mar 1, 1990 | F.A.S.T. TABLEK896583 · IXR | 510(k) clearances |
| Aug 10, 1989 | UROVIEW IIK893475 · JAA | 510(k) clearances |
| Jul 16, 1987 | UROVIEWK872022 · KQS | 510(k) clearances |
| Jan 30, 1987 | MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARMK864837 · JAA | 510(k) clearances |
| Jan 3, 1985 | ANGIOPLUS-SK843972 · JAA | 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
