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 |