The following data is part of a premarket notification filed by Kub Technologies, Inc. with the FDA for Kubtec Mozart Supra.
| Device ID | K200756 |
| 510k Number | K200756 |
| Device Name: | Kubtec Mozart Supra |
| Classification | Cabinet, X-ray System |
| Applicant | KUB Technologies, Inc. 111 Research Drive Stratford, CT 06615 |
| Contact | Chester Lowe |
| Correspondent | Chester Lowe KUB Technologies, Inc. 111 Research Drive Stratford, CT 06615 |
| Product Code | MWP |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-03-24 |
| Decision Date | 2020-06-12 |