Last synced on 14 November 2025 at 11:06 pm

Pre-Formed Extra Support Guidewire

Page Type
Cleared 510(K)
510(k) Number
K211741
510(k) Type
Traditional
Applicant
Lake Region Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2021
Days to Decision
168 days
Submission Type
Summary

Pre-Formed Extra Support Guidewire

Page Type
Cleared 510(K)
510(k) Number
K211741
510(k) Type
Traditional
Applicant
Lake Region Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2021
Days to Decision
168 days
Submission Type
Summary