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Cardicare Company, Ltd.

FDA Regulatory Profile

Cardicare Company, Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 28, 2022.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222652Aneroid Sphygmomanometer; Single Patient Use Aneroid SphygmomanometerNovember 28, 2022
K082542ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-ASeptember 17, 2008

FDA data resources