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EXPRESSWAY INTERMITTENT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K061766
510(k) Type
Traditional
Applicant
PERCUTANEOUS SYSTEMS, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/2007
Days to Decision
260 days
Submission Type
Summary

EXPRESSWAY INTERMITTENT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K061766
510(k) Type
Traditional
Applicant
PERCUTANEOUS SYSTEMS, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/2007
Days to Decision
260 days
Submission Type
Summary