Last synced on 14 November 2025 at 11:06 pm

RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K962472
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/1996
Days to Decision
63 days
Submission Type
Summary

RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K962472
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/1996
Days to Decision
63 days
Submission Type
Summary