Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled 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 ClearStream Technologies with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 12, 2011: BANTAM CATHETER (280MM BALLOON LENGTHS).
| Date | Record | Source |
|---|---|---|
| Oct 12, 2011 | BANTAM CATHETER (280MM BALLOON LENGTHS)K112335 · DQY | 510(k) clearances |
| Dec 1, 2010 | SLEEK OTW PTA CATHETERSK102035 · LIT | 510(k) clearances |
| Aug 4, 2010 | REEFLEX PTA CATHETERK101361 · LIT | 510(k) clearances |
| Mar 16, 2010 | LITEPAC, MODEL 682K100490 · LIT | 510(k) clearances |
| Dec 30, 2009 | BANTAM,48XXXXXX, 50XXXXXXK093139 · LIT | 510(k) clearances |
| Mar 2, 2009 | REEKROSS FAMILY OR OTW PTA CATHETERSK083596 · DQY | 510(k) clearances |
| Feb 8, 2008 | SAVVY LONG AND SLEEK PERIPHERAL TRANSLUMINAL ANGIOPLASTY (PTA) CATHETERSK072947 · LIT | 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