Diagnostics 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 Diacor, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jan 17, 2013: ZEPHYR 'X-SERIES PATIENT TRANSFER SLED.
| Date | Record | Source |
|---|---|---|
| Jan 17, 2013 | ZEPHYR 'X-SERIES PATIENT TRANSFER SLEDK121929 · FRZ | 510(k) clearances |
| May 23, 2005 | INTEGRA IMMOBILIZATION SYSTEMK050888 · IYE | 510(k) clearances |
| Oct 23, 1995 | CENTRALITE BACKPOINTERK954414 · IWE | 510(k) clearances |
| Sep 22, 1995 | PERI-PUSHERK953046 · IYE | 510(k) clearances |
| Aug 16, 1995 | CENTRALITE(R)-DLL SERIESK950112 · IWE | 510(k) clearances |
| Nov 3, 1993 | RADASSISTK934566 · IYE | 510(k) clearances |
| Jul 26, 1993 | MAMMORXK930246 · IYE | 510(k) clearances |
| Aug 17, 1989 | CENTRALITE BACKPOINTERK893398 · IWE | 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
