Last synced on 14 November 2025 at 11:06 pm

LiquID .051 LP Guide Catheter Extension

Page Type
Cleared 510(K)
510(k) Number
K243691
510(k) Type
Special
Applicant
Seigla Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2025
Days to Decision
129 days
Submission Type
Summary

LiquID .051 LP Guide Catheter Extension

Page Type
Cleared 510(K)
510(k) Number
K243691
510(k) Type
Special
Applicant
Seigla Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2025
Days to Decision
129 days
Submission Type
Summary