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Bionet Company, Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K023082
BABYCARE
March 3, 2003
K023034
CARDIOTOUCH-3000
November 14, 2002
K011328
CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPH
November 21, 2001