K110689 is an FDA 510(k) clearance for the INBODY. This device is classified as a Analyzer, Body Composition (Class II - Special Controls, product code MNW).
Submitted by Biospace Corporation Limited (Naples, US). The FDA issued a Cleared decision on August 19, 2011, 157 days after receiving the submission on March 15, 2011.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 870.2770.
| 510(k) Number | K110689 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 15, 2011 |
| Decision Date | August 19, 2011 |
| Days to Decision | 157 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | MNW — Analyzer, Body Composition |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2770 |