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VORTEK URETERAL DOUBLE LOOP STENT, BIOSOFT URETERAL DOUBLE LOOP STENT

Page Type
Cleared 510(K)
510(k) Number
K981591
510(k) Type
Special
Applicant
INTERNATIONAL REGULATORY CONSULTANTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1998
Days to Decision
158 days
Submission Type
Statement

VORTEK URETERAL DOUBLE LOOP STENT, BIOSOFT URETERAL DOUBLE LOOP STENT

Page Type
Cleared 510(K)
510(k) Number
K981591
510(k) Type
Special
Applicant
INTERNATIONAL REGULATORY CONSULTANTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1998
Days to Decision
158 days
Submission Type
Statement