K142833 is an FDA 510(k) clearance for the INTRAGen. This device is classified as a Skin Resurfacing Rf Applicator (Class II - Special Controls, product code OUH).
Submitted by Jeisys Medical, Inc. (Seoul, KR). The FDA issued a Cleared decision on June 4, 2015, 247 days after receiving the submission on September 30, 2014.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4400. Skin Resurfacing.
| 510(k) Number | K142833 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 30, 2014 |
| Decision Date | June 04, 2015 |
| Days to Decision | 247 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OUH - Skin Resurfacing Rf Applicator |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4400 |
| Definition | Skin Resurfacing |