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CYSTOGLIDE INTRODUCER SHEATH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052298
510(k) Type
Traditional
Applicant
PERCUTANEOUS SYSTEMS, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2006
Days to Decision
476 days
Submission Type
Summary

CYSTOGLIDE INTRODUCER SHEATH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052298
510(k) Type
Traditional
Applicant
PERCUTANEOUS SYSTEMS, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2006
Days to Decision
476 days
Submission Type
Summary