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IVT GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K911869
510(k) Type
Traditional
Applicant
INTENSIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1991
Days to Decision
173 days
Submission Type
Statement

IVT GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K911869
510(k) Type
Traditional
Applicant
INTENSIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1991
Days to Decision
173 days
Submission Type
Statement