Cleared Traditional

ML24000 UVA-1 PHOTOTHERAPY CABINET

K082731 · Daavlin Distributing Co. · General & Plastic Surgery
Dec 2008
Decision
90d
Days
Class 2
Risk

About This 510(k) Submission

K082731 is an FDA 510(k) clearance for the ML24000 UVA-1 PHOTOTHERAPY CABINET, a Light, Ultraviolet, Dermatological (Class II — Special Controls, product code FTC), submitted by Daavlin Distributing Co. (Bryan, US). The FDA issued a Cleared decision on December 17, 2008, 90 days after receiving the submission on September 18, 2008. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4630.

Submission Details

510(k) Number K082731 FDA.gov
FDA Decision Cleared SESE
Date Received September 18, 2008
Decision Date December 17, 2008
Days to Decision 90 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code FTC — Light, Ultraviolet, Dermatological
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4630

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