LipoFilter - Hospital Pack, LipoFilter - Clinic Pack— 510(k) K150779

Name: FDA 510(k) clearance K150779
Creator: U.S. Food and Drug Administration
Published: 2015-05-22

Substantially Equivalent

Microaire Surgical Instruments, LLC

FDA 510(k) clearance K150779 for LipoFilter - Hospital Pack, LipoFilter - Clinic Pack, Substantially Equivalent on 2015-05-22. Applicant: Microaire Surgical Instruments, LLC. Device class: 2.

Clearance details

Applicant: Microaire Surgical Instruments, LLC
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2015-03-25
Decision date: 2015-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Charlottesville, VA, 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 Microaire Surgical Instruments, LLC

view all

K243589 — PAL Sterilization Case2025-06-20
K244026 — PAL 7020 Console2025-04-25
K242804 — PAL Aspiration System2024-12-30
K220318 — PAL Infiltration System2022-10-14
K212024 — PAL System2022-06-10

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