Cleared Traditional

Biophotas Celluma CONTOUR

K232977 · Biophotas, Inc. · General & Plastic Surgery
Nov 2023
Decision
61d
Days
Class 2
Risk

About This 510(k) Submission

K232977 is an FDA 510(k) clearance for the Biophotas Celluma CONTOUR, a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Biophotas, Inc. (Tustin, US). The FDA issued a Cleared decision on November 21, 2023, 61 days after receiving the submission on September 21, 2023. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K232977 FDA.gov
FDA Decision Cleared SESE
Date Received September 21, 2023
Decision Date November 21, 2023
Days to Decision 61 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OLI — Fat Reducing Low Level Laser
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.5400
Definition Non-invasive Reduction In Fat Layer For Body Contouring

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