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MORSE(R) ANGIOGRAPHIC CATHETERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922552
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1993
Days to Decision
278 days
Submission Type
Statement

MORSE(R) ANGIOGRAPHIC CATHETERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922552
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/1993
Days to Decision
278 days
Submission Type
Statement