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VASCON NEUROPATH GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K052004
510(k) Type
Traditional
Applicant
VASCON LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2006
Days to Decision
178 days
Submission Type
Summary

VASCON NEUROPATH GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K052004
510(k) Type
Traditional
Applicant
VASCON LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2006
Days to Decision
178 days
Submission Type
Summary