Olympus Shirakawa Co., Ltd. is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Olympus Shirakawa Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PSD-60/ENDOPLASMA
1
Total
1
Cleared
0
Denied
Olympus Shirakawa 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: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Olympus Shirakawa Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Olympus Shirakawa Co., Ltd.
1 devices