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EXPRESSWAY INTERMITTENT CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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