FDA product code IMI

Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

Physical MedicineClass 221 CFR 890.5300

Verified

US regulatory classifications

US Product Code (FDA): IMI
US Risk Class (FDA): Class 2
US Regulation (CFR): 21 CFR 890.5300
Medical specialty: Physical Medicine

Device characteristics

GMP exempt: No
Implantable: No
Life-sustaining: No
Third party review: Eligible

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01Ultrasonic diathermy 02Therapeutic ultrasound 03Deep heat 04Physical therapy 05Pain relief 06Ultrasound therapy 07Therapeutic device 08Physiotherapy 09Heat therapy 10Ultrasound

About this record

Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat is a medical device type in the Physical Medicine specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.