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ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K926243
510(k) Type
Traditional
Applicant
TARGET THERAPEUTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1993
Days to Decision
248 days
Submission Type
Summary

ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K926243
510(k) Type
Traditional
Applicant
TARGET THERAPEUTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1993
Days to Decision
248 days
Submission Type
Summary