Last synced on 17 May 2024 at 11:06 pm

ARROW FlexBlock Continuous 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
K153652
510(k) Type
Traditional
Applicant
TELEFLEX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2016
Days to Decision
183 days
Submission Type
Summary

ARROW FlexBlock Continuous 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
K153652
510(k) Type
Traditional
Applicant
TELEFLEX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2016
Days to Decision
183 days
Submission Type
Summary