The following data is part of a premarket notification filed by Johnson & Johnson Consumer, Inc. with the FDA for Neutrogena Light Therapy Aging Mask+.
| Device ID | K180856 |
| 510k Number | K180856 |
| Device Name: | Neutrogena Light Therapy Aging Mask+ |
| Classification | Light Based Over The Counter Wrinkle Reduction |
| Applicant | Johnson & Johnson Consumer, Inc. 7050 Camp Hill Road Fort Washington, PA 19034 |
| Contact | Cindy R. Abraham |
| Correspondent | Cindy R. Abraham Johnson & Johnson Consumer, Inc. 7050 Camp Hill Road Fort Washington, PA 19034 |
| Product Code | OHS |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-04-02 |
| Decision Date | 2018-06-19 |
| Summary: | summary |