FDA 510(k) Applications Submitted by KUB TECHNOLOGIES, INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071233 | 05/03/2007 | XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM | KUB TECHNOLOGIES, INC |
| K083510 | 11/26/2008 | KUBTEC XPERT 20 | KUB TECHNOLOGIES, INC |
| K151221 | 05/07/2015 | Kubtec DIGIVIEW 395 | KUB TECHNOLOGIES, INC |
| K141539 | 06/10/2014 | KUBTEC X250 | KUB TECHNOLOGIES, INC |
| K103348 | 11/15/2010 | DIGIVIEW 250 | KUB TECHNOLOGIES, INC |
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