UINCARE HOME— 510(k) K172882

Substantially Equivalent

Uincare Corp.

FDA 510(k) clearance K172882 for UINCARE HOME, Substantially Equivalent on 2018-05-10. Applicant: Uincare Corp.. Device class: 2.

Clearance details

Applicant: Uincare Corp.
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 2017-09-21
Decision date: 2018-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geumcheon-Gu, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code LXJ

K192474 — VERA2019-10-10
K182333 — Vera2019-04-09
K180880 — DARI Health2019-03-07
K171547 — Qualisys Clinical System2018-08-02
K173931 — MindMotion(TM) GO2018-05-17

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