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LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension

Page Type
Cleared 510(K)
510(k) Number
K220691
510(k) Type
Traditional
Applicant
Seigla Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2022
Days to Decision
57 days
Submission Type
Summary

LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension

Page Type
Cleared 510(K)
510(k) Number
K220691
510(k) Type
Traditional
Applicant
Seigla Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2022
Days to Decision
57 days
Submission Type
Summary