BLU TOTALE (Model: ENEOB852)

FDA 510(k) K232656 · Premier North America, Inc.

Substantially Equivalent

510(k) numberK232656

Submission

Device name
BLU TOTALE (Model: ENEOB852)
Applicant
Premier North America, Inc.
Fort Lauderdale, FL, US
Received
August 31, 2023
Decision date
November 14, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OLP – Over-The-Counter Powered Light Based Laser For Acne
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

The device is intended for over-the-counter (otc) use to treat patients with mild to moderate acne vulgaris. The device is intended to emit energy in the red and blue region of the spectrum, specifically indicated to treat mild to moderate acne vulgaris.

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Questions and answers

When was BLU TOTALE (Model: ENEOB852) cleared by the FDA?

BLU TOTALE (Model: ENEOB852) (K232656) received a 510(k) decision of Substantially Equivalent on November 14, 2023, 75 days after the submission was received.

What is the product code of K232656?

The FDA product code is OLP – Over-The-Counter Powered Light Based Laser For Acne, a Class II (moderate risk) device regulated under 21 CFR 878.4810.