Medical Device Manufacturer · US , Hayward , CA

Pulse Biosciences, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2021

Total

Cleared

Denied

Pulse Biosciences, Inc. has 7 FDA 510(k) cleared medical devices. Based in Hayward, US.

Latest FDA clearance: Aug 2024. Active since 2021. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Pulse Biosciences, Inc. Filter by specialty or product code using the sidebar.

Pulse Biosciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pulse Biosciences, Inc.

7 devices

1-7 of 7