Multi III
FDA 510(k) K921953 · Excel Tech. , Ltd.
510(k) numberK921953
Submission
- Device name
- Multi III
- Applicant
- Excel Tech. , Ltd.
Oakville,Ontario, CA - Received
- April 27, 1992
- Decision date
- August 26, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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Questions and answers
When was Multi III cleared by the FDA?
Multi III (K921953) received a 510(k) decision of Substantially Equivalent on August 26, 1992, 121 days after the submission was received.
What is the product code of K921953?
The FDA product code is LIH – Interferential Current Therapy, a Class II (moderate risk) device regulated under 21 CFR 882.5890.