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POLYPLEX STIMULATING CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060186
510(k) Type
Traditional
Applicant
TE ME NA SAS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2006
Days to Decision
175 days
Submission Type
Summary

POLYPLEX STIMULATING CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060186
510(k) Type
Traditional
Applicant
TE ME NA SAS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2006
Days to Decision
175 days
Submission Type
Summary