510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K053451Substantially Equivalent

Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction Unit), Model 00 002 252 (220 V), 00 002 318 (110 V);

Moeller Medical GmbH & Co. KG, Coto De Caza CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K053451 is the FDA 510(k) clearance record for LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);, a class II device, cleared for Moeller Medical GmbH & Co. KG on under FDA product code QPB (System, Suction, Lipoplasty For Removal). FDA's definition for product code QPB reads: "A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring". FDA records list 2 510(k) clearances for Moeller Medical GmbH & Co. KG, from to . As of , FDA records show no recalls naming K053451.

Clearance record

Decision date
Received
(256 days to decision)
Product code
QPB System, Suction, Lipoplasty For Removal
Regulation
21 CFR 878.5040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Moeller Medical GmbH & Co. KG 23832 Via Monte, Coto De Caza CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QPB

Trailing 12 months
5 clearances under product code QPB in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QPB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20261
June 20261
July 20260
August 20261
September 20261
October 20260