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CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063061
510(k) Type
Traditional
Applicant
Viasys Medsystems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2007
Days to Decision
179 days
Submission Type
Statement

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063061
510(k) Type
Traditional
Applicant
Viasys Medsystems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2007
Days to Decision
179 days
Submission Type
Statement