Last synced on 2 December 2022 at 11:04 pm

URETHRA-BRUSH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942144
510(k) Type
Traditional
Applicant
ROVERS DIAGNOSTIC DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1994
Days to Decision
55 days
Submission Type
Summary

URETHRA-BRUSH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942144
510(k) Type
Traditional
Applicant
ROVERS DIAGNOSTIC DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1994
Days to Decision
55 days
Submission Type
Summary