FDA 510(k) Applications for Medical Device Product Code "NWB"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K133538 | OLYMPUS CORPORATION OF THE AMERICAS | VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2, VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE VA2, VISERA CYSTO-NE | 08/07/2014 |
K051645 | OLYMPUS MEDICAL SYSTEMS CORPORATION | EVIS EXERA 160A SYSTEM | 10/13/2005 |
K062049 | OLYMPUS MEDICAL SYSTEMS CORPORATION | EVIS EXERA II 180 SYSTEM | 09/22/2006 |
K072957 | OLYMPUS MEDICAL SYSTEMS CORPORATION | EVIS EXERA II 180 SYSTEM | 03/18/2008 |
K100584 | OLYMPUS MEDICAL SYSTEMS CORPORATION | EVIS EXERAII 180 SYSTEM | 07/02/2010 |
K090980 | OLYMPUS WINTER & IBE GMBH | HD ENDOEYE, MODELS WA50011A, WA50013A, WA50013L, WA50013T, WA50015L | 06/29/2009 |
K211882 | Sonoscape Medical Corp | HD-550 Video Endoscope System | 04/01/2022 |
K173921 | Sonoscape Medical Corp. | HD-500 Video Endoscope System | 09/05/2018 |
K222020 | Sonoscape Medical Corp. | HD-550 Video Endoscope System | 09/08/2022 |