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Liquet Medical, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K260149Versus™ Catheter (VS110-9NB)February 17, 2026
K241851Versus™ Catheter (VS110-8B)November 25, 2024