Pulse Biosciences, Inc.

Pulse Biosciences, Inc. holds 7 FDA 510(k) medical device clearances, first cleared 2021, most recent 2024.

Top product codes for Pulse Biosciences, Inc.

GEI — General, Plastic Surgery7 devices

Recent clearances by Pulse Biosciences, Inc.

K240782 — CellFX Percutaneous Electrode System (SYS3000) +2 moreCode GEI·2024-08-05
K233705 — CellFX Percutaneous Electrode System (SYS3000)Code GEI·2024-03-08
K213674 — CellFX SystemCode GEI·2022-09-22
K222075 — CellFX SystemCode GEI·2022-09-02
K221671 — CellFX® SystemCode GEI·2022-08-01
K211444 — CellFX SystemCode GEI·2021-08-25
K203299 — CellFX SystemCode GEI·2021-02-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.