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Medtek Devices, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K103375PLUMEPEN INTEGRATED SMOKE EVACUATION PENCILMarch 16, 2011
K052797LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUMFebruary 13, 2006