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VENTURE WIRE CONTROL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K040922
510(k) Type
Traditional
Applicant
Velocimed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2004
Days to Decision
132 days
Submission Type
Summary

VENTURE WIRE CONTROL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K040922
510(k) Type
Traditional
Applicant
Velocimed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2004
Days to Decision
132 days
Submission Type
Summary