Asahi Polyslider Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Asahi Polyslider Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: OneTouch Delica Safety, HemoCue Safety Lancet, Assure Lance and Assure Lance Plus, Capiject Safety Lancet, Heel Lancet Newborn, Heel Lancet Preemie, OneTouch Delica Plus Lancing System
2
Total
2
Cleared
0
Denied
Asahi Polyslider Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Maniwa, JP.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Asahi Polyslider Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo by UL as regulatory consultant.
FDA 510(k) Regulatory Record - Asahi Polyslider Co., Ltd.
2 devices