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ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set

Page Type
Cleared 510(K)
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)
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