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R2P Destination Slender Guiding Sheath

Page Type
Cleared 510(K)
510(k) Number
K171491
510(k) Type
Traditional
Applicant
Terumo Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2017
Days to Decision
136 days
Submission Type
Summary

R2P Destination Slender Guiding Sheath

Page Type
Cleared 510(K)
510(k) Number
K171491
510(k) Type
Traditional
Applicant
Terumo Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2017
Days to Decision
136 days
Submission Type
Summary