Arlington Scientific, Inc. (Asi) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arlington Scientific, Inc. (Asi) - FDA 510(k) Cleared Devices
Recent clearances: ASI Automated RPR (rapid plasma reagin) Test for Syphilis, for use on the ASI Evolution Automated Syphilis Analyzer, ASI Automated ASI RPR Test for Syphilis on the ASI Evolution, ASI Evolution
3
Total
3
Cleared
0
Denied
Arlington Scientific, Inc. (Asi) has 3 FDA 510(k) cleared medical devices. Based in Springville, US.
Historical record: 3 cleared submissions from 2018 to 2020. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Arlington Scientific, Inc. (Asi) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arlington Scientific, Inc. (Asi)
3 devices