GID 700— 510(k) K120902

Substantially Equivalent

The Gid Group, Inc.

FDA 510(k) clearance K120902 for GID 700, Substantially Equivalent on 2012-08-15. Applicant: The Gid Group, Inc.. Device class: 2.

Clearance details

Applicant: The Gid Group, Inc.
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2012-03-26
Decision date: 2012-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MUU

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

Recalls naming K120902

K-number listed on FDA's recall record

Z-0823-2018 — REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring.Class II·Terminated·LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC·20170808

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K120902.

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