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 15, 2026, FDA's public records list Cardiopulmonary Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 2013: BERNOULLI ENTERPRISE SOFTWARE.
| Dec 20, 2013 | BERNOULLI ENTERPRISE SOFTWAREK130208 · MHX | 510(k) clearances |
| Aug 14, 2009 | BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUEK091461 · MOD | 510(k) clearances |
| Sep 14, 2006 | BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWAREK061932 · MSX | 510(k) clearances |
| Jun 23, 2005 | MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWAREK051283 · MSX | 510(k) clearances |
| Feb 21, 2002 | MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWAREK020018 · MSX | 510(k) clearances |
| Nov 6, 2001 | BERNOULLI VENTILATOR MANAGEMENT SYSTEMK011861 · MOD | 510(k) clearances |
| Feb 24, 1999 | MODIFICATION OF VENTURI VENTILATORK990429 · CBK | 510(k) clearances |
| Jun 24, 1998 | VENTURI VENTILATORK982174 · CBK | 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
