DeviceClearance

Product code QPB— General, Plastic Surgery

ACCELERATOR RECIPROCATING CANNULA

Classification name
System, Suction, Lipoplasty For Removal
Device class
Class 2
Regulation
21 CFR 878.5040
Advisory panel
General, Plastic Surgery
Total cleared
60
First cleared
Most recent

FDA classification definition

“A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring”

— U.S. Food and Drug Administration, device classification record for product code QPB under 21 CFR 878.5040, via openFDA

Market context for product code QPB

FDA has cleared 60 devices under product code QPB between 1998 and 2026, filed by 39 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code QPB

Recent clearances under product code QPB

Data sourced from openFDA. This site is unofficial and independent of the FDA.