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TRANSRADIAL ARTERY ACCESS DEVICES

Page Type
Cleared 510(K)
510(k) Number
K112554
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2011
Days to Decision
77 days
Submission Type
Summary

TRANSRADIAL ARTERY ACCESS DEVICES

Page Type
Cleared 510(K)
510(k) Number
K112554
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2011
Days to Decision
77 days
Submission Type
Summary