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 |