Elcot, Inc.

FDA Regulatory Profile

Elcot, Inc. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Oct 18, 1991

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

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