FDA 510(k) Applications Submitted by FIEGERT-ENDOTECH MEDIZINTECHNIK GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K974493 11/28/1997 FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES FIEGERT-ENDOTECH MEDIZINTECHNIK GMBH


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