510(k) K120896
K120896 is an FDA 510(k) premarket notification submitted by Andon Health Co, Ltd. for the device "WI-FI BODY SCALE". The FDA issued a decision of Substantially Equivalent on July 26, 2012. The device falls under product code MNW (Analyzer, Body Composition), a Class II device regulated under 21 CFR 870.2770. Andon Health Co, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 26, 2012
- Date Received
- March 26, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Analyzer, Body Composition
- Device Class
- Class II
- Regulation Number
- 870.2770
- Review Panel
- GU
- Submission Type