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MULTITRACK ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K003902
510(k) Type
Special
Applicant
NUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2001
Days to Decision
23 days
Submission Type
Summary

MULTITRACK ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K003902
510(k) Type
Special
Applicant
NUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2001
Days to Decision
23 days
Submission Type
Summary