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Memtec Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K103427MOBILEECG SYSTEMMarch 24, 2011
K102723MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSISDecember 9, 2010
K944180MODEL 700March 7, 1997