Aicheck Biotech, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Aicheck Biotech, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Aicheck Biotech, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by LSI International, Inc. and Shanghai SUNGO Management Consulting Co., Ltd..
2 devices