Last synced on 14 November 2025 at 11:06 pm

UROSPROBE SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
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)
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