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LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K050168
510(k) Type
Traditional
Applicant
VASCULAR SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2005
Days to Decision
112 days
Submission Type
Summary

LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K050168
510(k) Type
Traditional
Applicant
VASCULAR SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2005
Days to Decision
112 days
Submission Type
Summary