LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200— 510(k) K092284

Name: FDA 510(k) clearance K092284
Creator: U.S. Food and Drug Administration
Published: 2009-09-01

Substantially Equivalent

Medical Device Resource Corp.

FDA 510(k) clearance K092284 for LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200, Substantially Equivalent on 2009-09-01. Applicant: Medical Device Resource Corp.. Device class: 2.

Clearance details

Applicant: Medical Device Resource Corp.
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2009-07-29
Decision date: 2009-09-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Hayward, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MUU

view all

K210528 — IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit2022-03-16
K203800 — SyntrFuge System2021-07-02
K202443 — Smart Kit Basic, Smart Kit Pro2021-03-11
K193539 — REVOLVE ENVI 600 Advanced Adipose System2020-05-28
K193363 — Dermapose Refresh2020-04-14

More clearances from Medical Device Resource Corp.

view all

K081593 — POWER ASPIRATOR, MODEL LS2 OR LS2DP2008-07-23

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