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K-Lok, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K935252K-LOK CATHETER SECUREMENT DEVICE MODIFICATIONFebruary 18, 1994
K930225K-LOK CATHETER SECUREMENT DEVICEApril 21, 1993