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COBE CATHETER W/GUIDEWIRE ASSEMBLY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853100
510(k) Type
Traditional
Applicant
COBE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1985
Days to Decision
64 days

COBE CATHETER W/GUIDEWIRE ASSEMBLY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853100
510(k) Type
Traditional
Applicant
COBE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1985
Days to Decision
64 days