Multi III, IV
FDA 510(k) K955860 · Excel Tech. , Ltd.
510(k) numberK955860
Submission
- Device name
- Multi III, IV
- Applicant
- Excel Tech. , Ltd.
Oakville,Ontario, CA - Received
- December 27, 1995
- Decision date
- March 22, 1996
- Decision
- Substantially Equivalent for Some Indications (SN)
- Type
- Traditional 510(k)
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Questions and answers
When was Multi III, IV cleared by the FDA?
Multi III, IV (K955860) received a 510(k) decision of Substantially Equivalent for Some Indications on March 22, 1996, 86 days after the submission was received.
What is the product code of K955860?
The FDA product code is LIH – Interferential Current Therapy, a Class II (moderate risk) device regulated under 21 CFR 882.5890.