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Kevtek Medical Products, Inc.

FDA Regulatory Profile

Kevtek Medical Products, 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 15, 1991.

Summary

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

Recent 510(k) Clearances

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

FDA data resources