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Vortex Medical, Inc.

FDA Regulatory Profile

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