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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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