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Cardiac Assist Devices, Inc.

FDA Regulatory Profile

Cardiac Assist Devices, 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 27, 2002.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K012520GYRO-TIP LARIAT DEFLECTABLE LOOP MAPPING CATHETER, MODEL GTL-20EMarch 27, 2002
K960849MAGNO ALARMMarch 26, 1997
K955847GYRO TIP EP CATHETERJanuary 29, 1997

FDA data resources