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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