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Proxis Ureteral Access Sheath

Page Type
Cleared 510(K)
510(k) Number
K160861
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2016
Days to Decision
2 days
Submission Type
Summary

Proxis Ureteral Access Sheath

Page Type
Cleared 510(K)
510(k) Number
K160861
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2016
Days to Decision
2 days
Submission Type
Summary