Last synced on 23 May 2025 at 11:06 pm

Vesair Cystoscopic Sheath

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162356
510(k) Type
Special
Applicant
Solace Therapeutics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2017
Days to Decision
191 days
Submission Type
Summary

Vesair Cystoscopic Sheath

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162356
510(k) Type
Special
Applicant
Solace Therapeutics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2017
Days to Decision
191 days
Submission Type
Summary