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 Deltec, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 23, 2003: CADD HIGH-VOLUME ADMINISTRATION SETS WITH FLOWSTOP.
| Date | Record | Source |
|---|---|---|
| May 23, 2003 | CADD HIGH-VOLUME ADMINISTRATION SETS WITH FLOWSTOPK031361 · FPA | 510(k) clearances |
| Apr 25, 2003 | TRUFLOW DUAL-LUMEN POLYURETHANE LONG-TERM STRAIGHT DIALYSIS CATHETER (12.5 FR X 24 CM) WITH TRAY, TRUFLOW DUAL-LUMEN POYK030983 · MSD | 510(k) clearances |
| Jan 30, 2003 | TRUFLOW LONG-TERM AND SHORT-TERM DUAL-LUMEN DIALYSIS CATHETERSK022221 · MPB | 510(k) clearances |
| Aug 13, 2002 | DELTEC INSULIN INFUSION PUMP AND ACCESSORIESK020655 · LZG | 510(k) clearances |
| Aug 13, 2002 | GRIPPER PLUS NEEDLEK021999 · FPA | 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
