MIDI-SRS— 510(k) K141046

Substantially Equivalent

Srmc Co., Ltd.

FDA 510(k) clearance K141046 for MIDI-SRS, Substantially Equivalent on 2014-12-24. Applicant: Srmc Co., Ltd.. Device class: 2.

Clearance details

Applicant: Srmc Co., Ltd.
Product code: Code ONG
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2014-04-23
Decision date: 2014-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fullerton, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ONG

K252155 — AVAVA Skin Treatment System2025-10-20
K244060 — eCO2 3D2025-07-31
K251031 — Fiber Laser Treatment Systems (HS-232,HS-233)2025-07-02
K250402 — AVAVA Skin Treatment System2025-04-14
K233550 — MOSAIC 3D (Surgical Laser)2024-01-02

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