FirmLabelled 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 Delphi Consulting Group with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 28, 1999: TRINITY II SINGLE CHAMBER DVT PUMP.
| Apr 28, 1999 | TRINITY II SINGLE CHAMBER DVT PUMPK983680 · JOW | 510(k) clearances |
| Nov 4, 1997 | TRINITY DVT SYSTEMK963957 · JOW | 510(k) clearances |
| Aug 6, 1997 | TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.)K970014 · JOW | 510(k) clearances |
| Dec 9, 1996 | SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEMK961937 · DQD | 510(k) clearances |
| Jun 11, 1996 | E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120K961301 · DQD | 510(k) clearances |
| Feb 22, 1996 | TRINITY SLEEVE(S)K954489 · JOW | 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
