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SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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