PULSE BIOSCIENCES, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30136868923013686892PULSE BIOSCIENCES, INC.1N2026-01-013957 Point Eden Way Hayward CA US 94545

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2879811131861535K240782CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX Percutaneous Electrode, 18G (CPE018)GEI2024-08-05
2879811896028808K233705CellFX Percutaneous Electrode System (SYS3000)GEI2024-03-08
2879811968931807K222075CellFX SystemGEI2022-09-02
2879811403160071K221671CellFX® SystemGEI2022-08-01
2879811309179309K213674CellFX SystemGEI2022-09-22
2879811244073740K211444CellFX SystemGEI2021-08-25
2879811583343224K203299CellFX SystemGEI2021-02-02

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI72024-08-05

PMN#

GUDID#