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Cimed Intl., Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K840766JANACEK TUBO-UTERINE IMPLANTATION SETApril 23, 1984
K833676SURGICAL VESSEL DILATORS-CATHERIZA-March 19, 1984
K833629CERTAIN MANUAL SURG. INSTRU. ACCESSJanuary 30, 1984