Rune Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rune Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rune Labs Tremor Transducer System
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.
FDA 510(k) Regulatory Record - Rune Labs, Inc.
1 devices