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MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100366
510(k) Type
Traditional
Applicant
MAXTER CATHETERS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/14/2010
Days to Decision
122 days
Submission Type
Summary