Cleared Traditional

Sensilight Pro / Pistol IPL

K183260 · El Global Trade, Ltd. · General & Plastic Surgery
Mar 2019
Decision
115d
Days
Class 2
Risk

About This 510(k) Submission

K183260 is an FDA 510(k) clearance for the Sensilight Pro / Pistol IPL, a Light Based Over-the-counter Hair Removal (Class II — Special Controls, product code OHT), submitted by El Global Trade, Ltd. (Netanya, IL). The FDA issued a Cleared decision on March 18, 2019, 115 days after receiving the submission on November 23, 2018. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.

Submission Details

510(k) Number K183260 FDA.gov
FDA Decision Cleared SESE
Date Received November 23, 2018
Decision Date March 18, 2019
Days to Decision 115 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OHT — Light Based Over-the-counter Hair Removal
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4810
Definition Over-the-counter Device Uses Thermal Energy To Kill Hair Follicles For Hair Removal.

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