Cardiopulmonary Corp.
Cardiopulmonary Corp. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2013.
Top product codes for Cardiopulmonary Corp.
Recent clearances by Cardiopulmonary Corp.
- K130208 — BERNOULLI ENTERPRISE SOFTWARE
- K091461 — BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUE
- K061932 — BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE
- K051283 — MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE
- K020018 — MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE
- K011861 — BERNOULLI VENTILATOR MANAGEMENT SYSTEM
- K990429 — MODIFICATION OF VENTURI VENTILATOR
- K982174 — VENTURI VENTILATOR
- K943412 — VENTURI VENTILATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.