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PERIPHERAL TRANSLUMINAL ANGIOPLASTY CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K971010
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1997
Days to Decision
90 days
Submission Type
Summary

PERIPHERAL TRANSLUMINAL ANGIOPLASTY CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K971010
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1997
Days to Decision
90 days
Submission Type
Summary