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BIOSOFT DUO DOUBLE LOOP URETERAL STENTS

Page Type
Cleared 510(K)
510(k) Number
K170422
510(k) Type
Traditional
Applicant
Coloplast Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2017
Days to Decision
262 days
Submission Type
Summary

BIOSOFT DUO DOUBLE LOOP URETERAL STENTS

Page Type
Cleared 510(K)
510(k) Number
K170422
510(k) Type
Traditional
Applicant
Coloplast Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2017
Days to Decision
262 days
Submission Type
Summary