Last synced on 14 November 2025 at 11:06 pm

BLADDERMANAGER PCI 5000 MODEL 1002

Page Type
Cleared 510(K)
510(k) Number
K982568
510(k) Type
Traditional
Applicant
DIAGNOSTIC ULTRASOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1999
Days to Decision
186 days
Submission Type
Summary

BLADDERMANAGER PCI 5000 MODEL 1002

Page Type
Cleared 510(K)
510(k) Number
K982568
510(k) Type
Traditional
Applicant
DIAGNOSTIC ULTRASOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1999
Days to Decision
186 days
Submission Type
Summary