Liposat Basic Infiltration Pump, Model 92-007 688
by Moeller Medical GmbH & Co. KG
510(k) K072793
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK072793 | Date4 Mar 2008 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- QPB
- Device Class
- Class II
- Regulation
- 21 CFR Part 878.5040
- Advisory Committee
- General, Plastic Surgery
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 1 Oct 2026
The Liposat Basic Infiltration Pump, Model 92-007 688, is a System, Suction, Lipoplasty for Removal device designed for use in lipoplasty procedures. It delivers controlled infiltration of fluids into subcutaneous tissue to facilitate liposuction by loosening fat deposits, aiding in their removal during suction-assisted lipoplasty. The device operates as part of a lipoplasty system, ensuring precise fluid administration to enhance surgical outcomes in body contouring procedures.
This device is supplied as a reusable medical instrument and is intended for use in sterile surgical settings. It is classified under FDA regulation 878.5040 as a Class II device with special controls, receiving FDA 510(k) clearance under the product code QPB. The Liposat Basic Infiltration Pump is intended for use in general and plastic surgery environments, adhering to standard infection control and sterilization protocols. Storage and handling must comply with manufacturer guidelines to maintain device integrity and functionality.
Other devices from Moeller Medical GmbH & Co. KG
Questions
AI-generated answers, 1 Oct 2026
What is the Liposat Basic Infiltration Pump used for?
The Liposat Basic Infiltration Pump, Model 92-007 688, is specifically designed for use in lipoplasty procedures. It controls the infiltration of fluids into subcutaneous tissue, which helps loosen fat deposits. This facilitates their removal during suction-assisted lipoplasty, improving surgical outcomes in body contouring.
Is the Liposat Basic Infiltration Pump reusable or single-use?
The Liposat Basic Infiltration Pump is supplied as a reusable medical instrument. It is intended for use in sterile surgical settings and must adhere to standard infection control and sterilization protocols to maintain its integrity and functionality.
What regulatory classification does the Liposat Basic Infiltration Pump hold?
The device is classified under FDA regulation 878.5040 as a Class II medical device with special controls. It received FDA 510(k) clearance under product code QPB, indicating it is deemed substantially equivalent to a predicate device.
How should the Liposat Basic Infiltration Pump be stored and handled?
The Liposat Basic Infiltration Pump must be stored and handled according to the manufacturer’s guidelines to ensure device integrity and functionality. Proper storage conditions are critical to maintain its performance and sterility, especially since it is intended for reuse in sterile surgical environments.
In which surgical environments is the Liposat Basic Infiltration Pump intended for use?
This device is intended for use in general and plastic surgery environments. It is designed to support lipoplasty procedures, ensuring precise fluid administration to enhance surgical outcomes in body contouring.