Last synced on 14 November 2025 at 11:06 pm

PathVisionXL

Page Type
Cleared 510(K)
510(k) Number
K183142
510(k) Type
Traditional
Applicant
Faxitron Bioptics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2019
Days to Decision
121 days
Submission Type
Summary

PathVisionXL

Page Type
Cleared 510(K)
510(k) Number
K183142
510(k) Type
Traditional
Applicant
Faxitron Bioptics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2019
Days to Decision
121 days
Submission Type
Summary