Cleared Traditional

MI-750 PROCEDURAL/MINOR SURGICAL LIGHT

K140812 · Medical Illumination International, Inc. · General & Plastic Surgery
Aug 2014
Decision
128d
Days
Class 2
Risk

About This 510(k) Submission

K140812 is an FDA 510(k) clearance for the MI-750 PROCEDURAL/MINOR SURGICAL LIGHT, a Light, Surgical, Ceiling Mounted (Class II — Special Controls, product code FSY), submitted by Medical Illumination International, Inc. (San Fernando, US). The FDA issued a Cleared decision on August 7, 2014, 128 days after receiving the submission on April 1, 2014. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4580.

Submission Details

510(k) Number K140812 FDA.gov
FDA Decision Cleared SESE
Date Received April 01, 2014
Decision Date August 07, 2014
Days to Decision 128 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code FSY — Light, Surgical, Ceiling Mounted
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4580