K200756 is an FDA 510(k) clearance for the Kubtec Mozart Supra. This device is classified as a Cabinet, X-ray System (Class II - Special Controls, product code MWP).
Submitted by Kub Technologies, Inc. (Stratford, US). The FDA issued a Cleared decision on June 12, 2020, 80 days after receiving the submission on March 24, 2020.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K200756 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 24, 2020 |
| Decision Date | June 12, 2020 |
| Days to Decision | 80 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | MWP - Cabinet, X-ray System |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |