Aicheck Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aicheck Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC, PocguideTM Multi-Drug Test Cup OTC, PocguideTM Multi-Drug Test Cup
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..
FDA 510(k) Regulatory Record - Aicheck Biotech, Inc.
2 devices