Compac a, Elite a, Elite a Plus, Surgica a

FDA 510(k) K913569 · Hgm Medical Laser Systems, Inc.

Substantially Equivalent

510(k) numberK913569

Submission

Device name
Compac a, Elite a, Elite a Plus, Surgica a
Applicant
Hgm Medical Laser Systems, Inc.
Salt Lake City, UT, US
Received
August 9, 1991
Decision date
October 17, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEX – Powered Laser Surgical Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue, for general surgical purpose in medical specialties of general and plastic surgery, dermatology/aesthetic, podiatry, otolaryngology (ent), gynecology…

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K261562Diode Laser Therapy SystemGEX · Traditional Sanhe LEFIS Electronics Co., Ltd.09/10/2026SE
K2615891927nm Thulium Laser System (PZ-DJG85-01, PZ-DJG85-02)GEX · Traditional Zhengzhou PZ Laser Slim Technology Co., Ltd.09/02/2026SE
K262269CO2 Laser System (MBT- CO2 Laser)GEX · Traditional Beijing Mega Beauty Technology Co., Ltd.09/01/2026SE
K2618211565nm Laser Therapy Device (PZ-JG86-01,PZ-JG86-02)GEX · Traditional Zhengzhou PZ Laser Slim Technology Co., Ltd.08/27/2026SE
K262070Diode Laser Therapy Systems (DL612A)GEX · Traditional Hebei Zollvan Medical Technology Co., Ltd.08/19/2026SE
K261964Echolaser X4GEX · Traditional Elesta S.P.A08/19/2026SE
K261841Q Switched Nd:YAG Laser machine (QLQW-01)GEX · Traditional Beijing Nubway S&T Co., Ltd.08/11/2026SE
K261221SOLTIVE™ Laser System (SOLTIVE™ Pro SuperPulsed Laser, SOLTIVE™ Premium SuperPulsed…GEX · Traditional Olympus Surgical Technologies America07/24/2026SE
K261738Medical Thulium Fiber Laser Systems (UroFiber 150Q)GEX · Traditional Rhein Laser Technologies Co., Ltd.07/21/2026SE

More from Rhein Laser Technologies Co., Ltd.

510(k)DeviceDecision
K921300Model PC Argon Ion LaserGEX · Traditional 10/06/1992SE
K914484Litespot(Tm) Laser Indirect OphthalmoscopeHLI · Traditional 01/06/1992SE
K912628Air Argon Ion Lasers Various ModelsGEX · Traditional 09/13/1991SE
K910272HGM Combination Nd:Yag & Solid State GreenGEX · Traditional 08/09/1991SE
K912438Models 5,8,20,20S Argon Ion LasersGEX · Traditional 07/17/1991SE
K910602HGM Argon Ion & Solid Light Laser for DentistryGEX · Traditional 06/24/1991SE
K911104Photcoagulator KR-568 Laser Spectrum Elite K1FEX · Traditional 06/11/1991SE
K910898Surgica(Tm) HGEX · Traditional 05/31/1991SE
K904699Compac(Tm) Diode LasersHQF · Traditional 04/25/1991SE
K904700Endocoagulator KRS568(TM) LaserGEX · Traditional 02/19/1991SE

Questions and answers

When was Compac a, Elite a, Elite a Plus, Surgica a cleared by the FDA?

Compac a, Elite a, Elite a Plus, Surgica a (K913569) received a 510(k) decision of Substantially Equivalent on October 17, 1991, 69 days after the submission was received.

What is the product code of K913569?

The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.