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Cortronic Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K884911
CORTRONIC SCR1000
January 13, 1989
K852547
CORTRONIC APM 770 NONINVASIVE & ARTERIAL PRESS MON
November 10, 1986