Stim2Go
K-Number: K230701 · 2023-11-24
Device Summary
Frequently Asked Questions
What is the Stim2Go?
Stim2Go is a medical device that received FDA 510(k) clearance on 2023-11-24. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K230701.
When did Stim2Go receive FDA 510(k) clearance?
Stim2Go received FDA 510(k) clearance on 2023-11-24, under 510(k) number K230701.
Who is the listed applicant for Stim2Go?
The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stim2Go?
The FDA product code for Stim2Go is IPF.
Other records listing PAJUNK GmbH Medizintechnologie as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IPF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.