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CORDIS CINCH(R) STEERABLE GUIDEWIRE EXT W/SLX COAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914863
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1991
Days to Decision
50 days
Submission Type
Statement

CORDIS CINCH(R) STEERABLE GUIDEWIRE EXT W/SLX COAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914863
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1991
Days to Decision
50 days
Submission Type
Statement