EGJ
- Product code
- EGJ
- Device name
- Device, Iontophoresis, Other Uses
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.5525
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 3
- Summaries archived here
- 3 (direct download)
- 510(k) clearances (all years, FDA)
- 73 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K242041 | 2025-04-01 | Taiwan Medical Electronics Co., Ltd. | STOPWET iontophoresis apparatus (SW01) | |
| K241267 | 2024-10-17 | Hidroxa Medical AB | Hidroxa SE30 | |
| K232020 | 2023-10-16 | Top-Rank Health Care Co., Ltd. | Iontophoresis Electrodes |
Official FDA classification page: EGJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).