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ENDOVIVE LOW PROFILE REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX, 8283, 8284, 8285

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083685
510(k) Type
Traditional
Applicant
MRI MANUFACTURING AND RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2009
Days to Decision
195 days
Submission Type
Summary