Sakura Seiki Co., Ltd. is one of 18904 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sakura Seiki Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SAKURA STEAM STERILIZER ASSR, SAKURA STEAM STERILIZAER MODEL ASSV-AH06, SKYRON INTEGRITY 215 STEAM STERILIZER SKYTRON INTEGRITY 215 SG STEAM STERILIZER SAKURA STEAM STERILIZER ASSV-AB09 SAKURA
3
Total
3
Cleared
0
Denied
Sakura Seiki Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 3 cleared submissions from 2012 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sakura Seiki Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sakura Seiki Co., Ltd.
3 devices