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ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65

Page Type
Cleared 510(K)
510(k) Number
K981191
510(k) Type
Traditional
Applicant
INTRATHERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1999
Days to Decision
370 days
Submission Type
Summary

ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65

Page Type
Cleared 510(K)
510(k) Number
K981191
510(k) Type
Traditional
Applicant
INTRATHERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1999
Days to Decision
370 days
Submission Type
Summary