The following data is part of a premarket notification filed by Radiancy (israel) Ltd. with the FDA for Radiancy Facial Skincare Device.
| Device ID | K052991 |
| 510k Number | K052991 |
| Device Name: | RADIANCY FACIAL SKINCARE DEVICE |
| Classification | Powered Laser Surgical Instrument |
| Applicant | RADIANCY (ISRAEL) LTD. 40 RAMLAND ROAD SUITE 10 Orangeburg, NY 10962 |
| Contact | Margaret Fourte |
| Correspondent | Margaret Fourte RADIANCY (ISRAEL) LTD. 40 RAMLAND ROAD SUITE 10 Orangeburg, NY 10962 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-10-25 |
| Decision Date | 2006-02-01 |
| Summary: | summary |