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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Catheter Connections, Inc. with 7 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated May 22, 2015: DualCap.
| May 22, 2015 | DualCapK142806 · QBP | 510(k) clearances |
| Nov 19, 2014 | DualCap IV Pole Strips(Disinfectant Caps for Male Luers)K142399 · QBP | 510(k) clearances |
| Aug 5, 2014 | DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB, Sterile. When left in place for five (5) minutes DualCap SolClass II · Catheter Connections is recalling DualCap IV Pole Strips disinfectant caps for luer access valves due to potential impro | Device recalls |
| Jan 22, 2013 | CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERSK123967 · QBP | 510(k) clearances |
| Dec 14, 2012 | CATHETER CONNECTIONS DUALCAP SOLOK123065 · QBP | 510(k) clearances |
| Jan 27, 2012 | CATHETER CONNECTIONS' DUALCAP SOLOK113842 · QBP | 510(k) clearances |
| Nov 9, 2011 | CATHETER CONNECTIONS' DUALCAP DUOK112985 · QBP | 510(k) clearances |
| Apr 8, 2010 | CATHETER CONNECTIONS DUALCAPK093229 · QBP | 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
