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Kevtek Medical Products, Inc.

FDA Regulatory Profile

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

Latest 510(k)
Mar 15, 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 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K902193KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOPMar 15, 1991
K902000KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELDAug 21, 1990

FDA data resources