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Seigla Medical, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K243691LiquID .051 LP Guide Catheter ExtensionApril 4, 2025
K220691LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter ExtensionMay 5, 2022