Stim2Go
by Pajunk GmbH Medizintechnologie
510(k) K230701
Stim2Go is a medical device (FDA Class II; FDA product code IPF, Stimulator, Muscle, Powered) made by Pajunk GmbH Medizintechnologie, cleared under FDA 510(k) K230701 on 24 Nov 2023, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK230701 | Date24 Nov 2023 | StatusActive |
Official records
- FDA 510(k) database K230701
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IPF
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5850
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K230701
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Stim2Go 9151-10-00 | 9151-10-00 / 9151-10-00 | 04048223122235 | — | On the market |
Similar devices
Other devices filed under FDA product code IPF (Stimulator, Muscle, Powered).
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