K121800 is an FDA 510(k) clearance for the POINT 500 HD POINT500C HD. This device is classified as a System, X-ray, Extraoral Source, Digital (Class II - Special Controls, product code MUH).
Submitted by Pointnix Co., Ltd. (Great Neck, US). The FDA issued a Cleared decision on January 24, 2013, 219 days after receiving the submission on June 19, 2012.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 872.1800.
| 510(k) Number | K121800 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 19, 2012 |
| Decision Date | January 24, 2013 |
| Days to Decision | 219 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | MUH - System, X-ray, Extraoral Source, Digital |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.1800 |