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Medtek Devices, Inc.

FDA Regulatory Profile

Medtek Devices, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 16, 2011.

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

FDA data resources