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FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140110
510(k) Type
Traditional
Applicant
TELEFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2015
Days to Decision
436 days
Submission Type
Summary

FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140110
510(k) Type
Traditional
Applicant
TELEFLEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2015
Days to Decision
436 days
Submission Type
Summary