Zeptometrix - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Zeptometrix has 1 FDA 510(k) cleared medical devices. Based in Buffalo, US.
Last cleared in 2022. Active since 2022. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Zeptometrix Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MDC Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Zeptometrix
1 devices