FDA 510(k)

Stim2Go

K-Number: K230701 · 2023-11-24

Decision Date2023-11-24

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Stim2Go is a medical device manufactured by PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2023-11-24 under approval number K230701. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stim2Go?

Stim2Go is a medical device that received FDA 510(k) clearance on 2023-11-24. It is manufactured by PAJUNK GmbH Medizintechnologie. The 510(k) number is K230701.

When was Stim2Go approved by the FDA?

Stim2Go received FDA 510(k) clearance on 2023-11-24, under approval number K230701.

What company makes Stim2Go?

Stim2Go is manufactured by PAJUNK GmbH Medizintechnologie.

What is the FDA product code for Stim2Go?

The FDA product code for Stim2Go is IPF.

Other Devices by PAJUNK GmbH Medizintechnologie

K160297Tuohy NRFit K160295SPROTTE NRFit, Quincke NRFit K160296SPROTTE SPECIAL NRFit K160294SPROTTE NRFit, Quincke NRFit Lumbar Puncture needles K152952E-Cath K170305Spinal Manometer NRFit; Spinal Manometer LUER

View all 21 devices →

Related Devices (Code: IPF)

K160614Xcite Clinical StationRestorative Therapies, Inc. K163067CyMedica e-vive System; CY-1000Cymedica Orthopedics, Inc. K160992HPM-6000BTL Industries, Inc. K151922StimSox(TM) SystemStimmed, LLC K153696Chattanooga Revolution WirelessDjo, LLC K160299geko(TM) Plus R-2 Neuromuscular StimulatorFirstkind Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.