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VERITRACT ENTERAL FEEDING TUBE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133334
510(k) Type
Traditional
Applicant
VERITRACT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2014
Days to Decision
301 days
Submission Type
Statement