Last synced on 25 November 2022 at 11:04 pm

Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190099
510(k) Type
Traditional
Applicant
Corinth MedTech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2019
Days to Decision
52 days
Submission Type
Summary

Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190099
510(k) Type
Traditional
Applicant
Corinth MedTech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2019
Days to Decision
52 days
Submission Type
Summary