The following data is part of a premarket notification filed by Quest Medical, Inc. with the FDA for Liposol.
| Device ID | K830472 |
| 510k Number | K830472 |
| Device Name: | LIPOSOL |
| Classification | Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Applicant | QUEST MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JKA |
| CFR Regulation Number | 862.1675 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-15 |
| Decision Date | 1983-06-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LIPOSOL 77211230 3592105 Live/Registered |
SABINSA CORPORATION 2007-06-20 |
![]() LIPOSOL 74011133 not registered Dead/Abandoned |
PROFESSIONAL NUTRITION MANAGEMENT, LTD. 1989-12-15 |
![]() LIPOSOL 73463265 1316383 Live/Registered |
Biosol, Ltd. 1984-01-27 |