The following data is part of a premarket notification filed by Pretika Corporation with the FDA for Soniclift.
| Device ID | K150077 |
| 510k Number | K150077 |
| Device Name: | SonicLift |
| Classification | Stimulator, Transcutaneous Electrical, Aesthetic Purposes |
| Applicant | PRETIKA CORPORATION 12215 Holly Street Riverside, CA 92509 |
| Contact | Thomas Nichols |
| Correspondent | Thomas Nichols PRETIKA CORPORATION 12215 Holly Street Riverside, CA 92509 |
| Product Code | NFO |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-01-14 |
| Decision Date | 2015-11-25 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SONICLIFT 85460751 4223227 Live/Registered |
Pretika Corporation 2011-10-31 |
![]() SONICLIFT 77305986 not registered Dead/Abandoned |
Brennan, Dr. William A. 2007-10-17 |