Vortex Medical, Inc.

FDA Regulatory Profile

Vortex Medical, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 5, 2014.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K133445ANGIOVAC CANNULAMarch 5, 2014
K092486VORTEX MEDICAL ANGIOVAC CARDIOPULMONARY BYPASS CIRCUITAugust 28, 2009
K091304VORTEX CANNULAJuly 2, 2009