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IMJ

Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

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)
3
Summaries archived here
3 (direct download)
510(k) clearances (all years, FDA)
45 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (3)

Last three years. Most recent: 2026-06-12.

NumberDecision dateApplicantDevice nameSummary
K2529632026-06-12BTL Industries, Inc.BTL-899TTPDF
K2503762025-11-05Viatherm Therapeutics, LLCViVYPDF
K2431122025-06-25Enraf-Nonius, B.V.Curapuls 670PDF

3 summaries are archived here for direct download.

Official FDA classification page: IMJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).