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Icn Micromedic Systems
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K884269
SAMPLE IDENTIFICATION STATION MODEL 38010
January 9, 1989
K883746
MICROMEDIC FERRITIN IRMA KIT
October 27, 1988
K880674
MICROMEDIC CRACKPOT RIA KIT
October 6, 1988
K881102
MICROMEDIC MORPHINE RIA KIT
June 24, 1988