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FDA 510(k) Applications Submitted by SUZANNE DEW
FDA 510(k) Number
Submission Date
Device Name
Applicant
K083684
12/12/2008
ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX
MANUFACTURING & RESEARCH, INC.
K083685
12/12/2008
ENDOVIVE LOW PROFILE REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX, 8283, 8284, 8285
MRI MANUFACTURING AND RESEARCH, INC.
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