FDA 510(k) Applications Submitted by OLYMPUS CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K072643 09/18/2007 CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US OLYMPUS CORPORATION
K040940 04/12/2004 BRONCHOVIDEOSCOPE OLYMPUS XBF-D160HM OLYMPUS CORPORATION
K041494 06/04/2004 OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA (CONTROL UNIT FOR ENDOSURGERY UCES-2) SOFTWARE VERSION 2 OLYMPUS CORPORATION
K042140 08/09/2004 OLYMPUS BF TYPE UC160-OL8 OLYMPUS CORPORATION
K043128 11/12/2004 OLYMPUS ENDOARM OLYMPUS CORPORATION


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