The following data is part of a premarket notification filed by Kub Technologies, Inc with the FDA for Kubtec X250.
| Device ID | K141539 |
| 510k Number | K141539 |
| Device Name: | KUBTEC X250 |
| Classification | System, X-ray, Mobile |
| Applicant | KUB TECHNOLOGIES, INC 270 ROWE AVENUE, UNIT E Milford, CT 06461 |
| Contact | Vikram Butani |
| Correspondent | Vikram Butani KUB TECHNOLOGIES, INC 270 ROWE AVENUE, UNIT E Milford, CT 06461 |
| Product Code | IZL |
| CFR Regulation Number | 892.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-06-10 |
| Decision Date | 2014-10-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B619KUB2500 | K141539 | 000 |