BK200539 - ASI Automated RPR test for Syphilis for use on the ASI Evolution
510(k) Number: BK200539
Applicant: Arlington Scientific, Inc.
Device Name: ASI Automated RPR test for Syphilis for use on the ASI Evolution
Decision Date: 2/2/2021
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: BK200539
Applicant: Arlington Scientific, Inc.
Device Name: ASI Automated RPR test for Syphilis for use on the ASI Evolution
Decision Date: 2/2/2021