Last synced on 18 April 2025 at 11:05 pm

PTFE Guidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242824
510(k) Type
Special
Applicant
Lake Region Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2024
Days to Decision
79 days
Submission Type
Summary

PTFE Guidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242824
510(k) Type
Special
Applicant
Lake Region Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2024
Days to Decision
79 days
Submission Type
Summary