Medical Diode Laser Systems

FDA 510(k) K230047 · Gigaalaser Company , Ltd.

Substantially Equivalent

510(k) numberK230047

Submission

Device name
Medical Diode Laser Systems
Applicant
Gigaalaser Company , Ltd.
Wuhan, CN
Received
January 6, 2023
Decision date
March 4, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NVK – Laser, Dental, Soft Tissue
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

Intended for the incision, excision, cutting, ablation, and vaporization of soft tissue in oral and maxillofacial surgery and dentistry.

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Questions and answers

When was Medical Diode Laser Systems cleared by the FDA?

Medical Diode Laser Systems (K230047) received a 510(k) decision of Substantially Equivalent on March 4, 2024, 423 days after the submission was received.

What is the product code of K230047?

The FDA product code is NVK – Laser, Dental, Soft Tissue, a Class II (moderate risk) device regulated under 21 CFR 878.4810.