Avecor Cardiovascular, Inc.
Avecor Cardiovascular, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 1998.
Top product codes for Avecor Cardiovascular, Inc.
Recent clearances by Avecor Cardiovascular, Inc.
- K973760 — AFFINITY HOLLOW FIBER OXYGENATOR WITH TRILLIUM BIOPASSIVE SURFACE
- K964017 — AFFINITY BLOOD PUMP SYSTEM
- K971105 — MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM
- K952532 — AFFINITY ARTERIAL BLOOD FILTER
- K940126 — AVECOR PRE-BYPASS FILTER
- K936003 — AFFINITY CVR
- K935717 — AFFINITY VENOUS RESERVIOR BAG
- K932252 — AFFINITY HOLLOW FIBER OXYGENATOR
- K924529 — SIGNATURE(TM) CUSTOM TUBING PACK
Data sourced from openFDA. This site is unofficial and independent of the FDA.