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Gemini, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K810870GEMENI CK-MB ISOENZYME ABNORMAL SERUMApril 14, 1981
K810534GEMENI QUICK-MB SEPARATION KITMarch 11, 1981