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Elcot, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K911144MF-500, MODIFICATIONOctober 18, 1991
K863815ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000June 2, 1987