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SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)

Page Type
Cleared 510(K)
510(k) Number
K960801
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1996
Days to Decision
31 days
Submission Type
Summary

SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)

Page Type
Cleared 510(K)
510(k) Number
K960801
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1996
Days to Decision
31 days
Submission Type
Summary