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FDA 510(k) Applications Submitted by ERIC MAYNARD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120084
01/11/2012
ENDOSCOPIC RETRIEVAL DEVICE
UNITED STATES ENDOSCOPY GROUP, INC.
K131598
06/03/2013
ANAL RECTAL OVERTUBE
UNITED STATES ENDOSCOPY GROUP, INC.
K133736
12/09/2013
ENDOSCOPIC SUTURE CUTTER
UNITED STATES ENDOSCOPY GROUP, INC.
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