Acro Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acro Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Acro HCG Pregnancy Rapid Test, ACRO HCG Pregnancy Rapid Test
2
Total
2
Cleared
0
Denied
Acro Biotech, Inc. has 2 FDA 510(k) cleared medical devices. Based in Rancho Cucamonga, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Acro Biotech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ivdd Regulatory Consultant as regulatory consultant.
FDA 510(k) Regulatory Record - Acro Biotech, Inc.
2 devices