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INTRAMAX ITI GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992622
510(k) Type
Special
Applicant
INTRATHERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1999
Days to Decision
55 days
Submission Type
Summary

INTRAMAX ITI GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992622
510(k) Type
Special
Applicant
INTRATHERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1999
Days to Decision
55 days
Submission Type
Summary