Rune Labs, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Rune Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Rune Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Anacapa Clinical Research, Inc. as regulatory consultant.
1 devices