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DIRECTVISION CATHETER, UNCOATED

Page Type
Cleared 510(K)
510(k) Number
K110214
510(k) Type
Special
Applicant
PERCUVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2011
Days to Decision
122 days
Submission Type
Summary

DIRECTVISION CATHETER, UNCOATED

Page Type
Cleared 510(K)
510(k) Number
K110214
510(k) Type
Special
Applicant
PERCUVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2011
Days to Decision
122 days
Submission Type
Summary