LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V)— 510(k) K053451

Name: FDA 510(k) clearance K053451
Creator: U.S. Food and Drug Administration
Published: 2006-08-25

Substantially Equivalent

Moeller Medical GmbH & Co. KG

FDA 510(k) clearance K053451 for LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V), Substantially Equivalent on 2006-08-25. Applicant: Moeller Medical GmbH & Co. KG. Device class: 2.

Clearance details

Device name as filed: LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);
Applicant: Moeller Medical GmbH & Co. KG
Product code: Code QPB
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2005-12-12
Decision date: 2006-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Coto De Caza, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QPB

view all

K254135 — LipoSurg ARTIST2026-09-05
K261710 — AYON Power Liposuction Cannulas and AYON Power Liposuction Cannula Adaptors2026-08-21
K251944 — Lipocosm Harmonic System2026-06-08
K253396 — AYON Body Contouring System (AYON SYSTEM)2026-05-08
K252495 — LSSA (NP-200)2026-04-03

More clearances from Moeller Medical GmbH & Co. KG

view all

K072793 — LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 6882008-03-04

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