Last synced on 18 April 2025 at 11:05 pm

LiquID .051 LP Guide Catheter Extension

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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