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Mecta Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K965070SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.March 6, 1997
K960754SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 MSeptember 18, 1996
K852069MECTA ECT DEVICE MODELS SR & JRAugust 9, 1985