The following data is part of a premarket notification filed by Precision Dermatology Incorporated with the FDA for Hylatopicplus Lotion.
| Device ID | K121559 |
| 510k Number | K121559 |
| Device Name: | HYLATOPICPLUS LOTION |
| Classification | Dressing, Wound, Drug |
| Applicant | PRECISION DERMATOLOGY INCORPORATED 900 HIGHLAND CORPORATE DRIVE Cumberland, RI 02864 |
| Contact | Ronald M Gurge |
| Correspondent | Ronald M Gurge PRECISION DERMATOLOGY INCORPORATED 900 HIGHLAND CORPORATE DRIVE Cumberland, RI 02864 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-05-29 |
| Decision Date | 2012-11-30 |
| Summary: | summary |