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 Cardiovascular Dynamics with 11 510(k) clearances. The most recent is a 510(k) clearance dated Jan 23, 1998: 22 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CATHETER/NEEDLE ASSEMBLY), 24 GAUGE P.D. AC….
| Jan 23, 1998 | 22 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CATHETER/NEEDLE ASSEMBLY), 24 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CARK973713 · ITX | 510(k) clearances |
| Jun 18, 1997 | FOCUS-PV BALLOON DILATATION CATHETERK971577 · LIT | 510(k) clearances |
| Apr 24, 1997 | P.D. ACCESS (PERCUTANEOUS DOPPLER) VASCULAR ACCESS DEVICEK963989 · ITX | 510(k) clearances |
| Mar 28, 1997 | FOCUS PV BALLOON DILATATION CATHETERK963688 · LIT | 510(k) clearances |
| Aug 17, 1995 | CVD PERIFLOW(TM) (SMALL VESSEL) BALLOON DILATATION CATHETERK945693 · LIT | 510(k) clearances |
| Jun 21, 1995 | FOCUS BALLOON DILATATION CATHETERK952064 · LIT | 510(k) clearances |
| May 10, 1995 | CVD BULLET INFUSION CATYHETERK951502 · KRA | 510(k) clearances |
| May 4, 1995 | CVD BULLETT HI-FLO INFUSION CATHETERK951503 · KRA | 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
