Last synced on 25 January 2026 at 3:41 am

UROSPROBE SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960387
510(k) Type
Traditional
Applicant
Uros Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1996
Days to Decision
66 days
Submission Type
Statement

UROSPROBE SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960387
510(k) Type
Traditional
Applicant
Uros Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1996
Days to Decision
66 days
Submission Type
Statement