Model 25 Therapeutic Ultrasound -- Modified

FDA 510(k) K923797 · Rich-Mar Corp.

Substantially Equivalent

510(k) numberK923797

Submission

Device name
Model 25 Therapeutic Ultrasound -- Modified
Applicant
Rich-Mar Corp.
Inola, OK, US
Received
July 28, 1992
Decision date
November 6, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
IMG – Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5860
Specialty
Physical Medicine

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Questions and answers

When was Model 25 Therapeutic Ultrasound -- Modified cleared by the FDA?

Model 25 Therapeutic Ultrasound -- Modified (K923797) received a 510(k) decision of Substantially Equivalent on November 6, 1992, 101 days after the submission was received.

What is the product code of K923797?

The FDA product code is IMG – Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat, a Class II (moderate risk) device regulated under 21 CFR 890.5860.