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MODIFICATION TO CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080679
510(k) Type
Traditional
Applicant
VIASYS MEDSYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2008
Days to Decision
109 days
Submission Type
Statement