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MODIFICATION TO ENDOVASCULAR GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K043457
510(k) Type
Special
Applicant
Stereotaxis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2005
Days to Decision
75 days
Submission Type
Summary

MODIFICATION TO ENDOVASCULAR GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K043457
510(k) Type
Special
Applicant
Stereotaxis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2005
Days to Decision
75 days
Submission Type
Summary