IMJ
- Product code
- IMJ
- Device name
- Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.5290
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 45
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K252963 | 2026-06-12 | BTL Industries, Inc. | BTL-899TT | |
| K250376 | 2025-11-05 | Viatherm Therapeutics, LLC | ViVY | |
| K243112 | 2025-06-25 | Enraf-Nonius, B.V. | Curapuls 670 |
Official FDA classification page: IMJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).