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CORDIS NITINOL STENT AND DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980823
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/18/1998
Days to Decision
290 days
Submission Type
Summary

CORDIS NITINOL STENT AND DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980823
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/18/1998
Days to Decision
290 days
Submission Type
Summary