Asahi Kasei Pharma Corporation is one of 128 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Asahi Kasei Pharma Corporation - FDA 510(k) Cleared Devices
Recent clearances: Lucica Glycated Albumin-L
1
Total
1
Cleared
0
Denied
Asahi Kasei Pharma Corporation has 1 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Asahi Kasei Pharma Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Quintilesims as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Asahi Kasei Pharma Corporation
1 devices