Last synced on 14 November 2025 at 11:06 pm

Amplatzer Guidewire

Page Type
Cleared 510(K)
510(k) Number
K250031
510(k) Type
Traditional
Applicant
Abbott Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2025
Days to Decision
269 days
Submission Type
Summary

Amplatzer Guidewire

Page Type
Cleared 510(K)
510(k) Number
K250031
510(k) Type
Traditional
Applicant
Abbott Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2025
Days to Decision
269 days
Submission Type
Summary