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Cardio Search, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K842133
EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS
February 19, 1985
K841880
ERYTHROCATH UMBILICAL CATHETER
January 14, 1985
K833873
CARDIOSEARCH RIGHT ATRIAL CATH-
June 11, 1984
K832064
VENOUS CATHETER
August 8, 1983