Aizu Olympus Co., Ltd. is one of 15076 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aizu Olympus Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EVIS EXERA COLONOVIDEOSCOPE MODEL XCF-Q160W1L/1
1
Total
1
Cleared
0
Denied
Aizu Olympus Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Melville, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Aizu Olympus Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Aizu Olympus Co., Ltd.
1 devices