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 Advanced Instrument Development, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 17, 1998: IMIX DIGITAL THORAX SYSTEM.
| Date | Record | Source |
|---|---|---|
| Mar 17, 1998 | IMIX DIGITAL THORAX SYSTEMK974863 · KPR | 510(k) clearances |
| Aug 12, 1987 | POWER-AID INDEPENDENT X-RAY POWER SOURCEK872445 · IZO | 510(k) clearances |
| Jun 18, 1982 | AUTOMATIC EXPOSURE CONTROL TYPE A3300K827525 · | 510(k) clearances |
| Dec 3, 1981 | MOBIL-AID AUTOMATIC EXPOSURE CONTROLK813128 · IZL | 510(k) clearances |
| Nov 13, 1979 | CONVERSION CONTRACTOR TIMER KITK791933 · IZO | 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
