The following data is part of a premarket notification filed by Puregraft Llc with the FDA for Dermapose Refresh.
| Device ID | K193363 |
| 510k Number | K193363 |
| Device Name: | Dermapose Refresh |
| Classification | System, Suction, Lipoplasty |
| Applicant | Puregraft LLC 420 Stevens Avenue, Suite 220 Solana Beach, CA 92075 |
| Contact | Olivia Kim |
| Correspondent | Olivia Kim Puregraft LLC 420 Stevens Avenue, Suite 220 Solana Beach, CA 92075 |
| Product Code | MUU |
| CFR Regulation Number | 878.5040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-12-04 |
| Decision Date | 2020-04-14 |