Last synced on 14 November 2025 at 11:06 pm

Autofuse

Page Type
Cleared 510(K)
510(k) Number
K233572
510(k) Type
Traditional
Applicant
Pymedix
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2024
Days to Decision
121 days
Submission Type
Summary

Autofuse

Page Type
Cleared 510(K)
510(k) Number
K233572
510(k) Type
Traditional
Applicant
Pymedix
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2024
Days to Decision
121 days
Submission Type
Summary