FDA 510(k) Applications Submitted by MAX ENDOSCOPY INC.

FDA 510(k) Number Submission Date Device Name Applicant
K083275 11/06/2008 PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE- USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2 MAX ENDOSCOPY INC.
K080764 03/18/2008 SUCCESS CECAL INTUBATION ASSIST, MODEL: 4100 MAX ENDOSCOPY INC.


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