Site 810E Photocoagulator and Accessories

FDA 510(k) K895663 · Site Microsurgical Systems, Inc.

Substantially Equivalent

510(k) numberK895663

Submission

Device name
Site 810E Photocoagulator and Accessories
Applicant
Site Microsurgical Systems, Inc.
Horsham, PA, US
Received
September 20, 1989
Decision date
December 4, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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
K925828Modified Site TXR SystemsHQC · Traditional 02/16/1994SE
K925921Modified Site Disposable Diaphragm CassetteKYG · Traditional 12/06/1993SE
K931866Site's CD II Phacoemulsification HandpieceHQC · Traditional 11/12/1993SE
K921135Iolab Power I.V. PoleHQC · Traditional 06/03/1992SE
K920582180 Tip, 1/A Handpiece .3MM End Opening for Opht.HQE · Traditional 05/08/1992SE
K912902Phacoemulsification System for Ophthalmic UseHQC · Traditional 12/17/1991SE
K912739Site 90 Tip, I/A Handpiece .3MM Side Open/Opth UseHQC · Traditional 08/28/1991SE
K910980Site 20 Gauge Reusable Fiber Optic CableHJO · Traditional 05/22/1991SE
K905620Modified Site Peristaltic FootswitchEBW · Traditional 02/27/1991SE
K904183Site Phacoemulsification HandpieceHQC · Traditional 12/05/1990SE

Questions and answers

When was Site 810E Photocoagulator and Accessories cleared by the FDA?

Site 810E Photocoagulator and Accessories (K895663) received a 510(k) decision of Substantially Equivalent on December 4, 1989, 75 days after the submission was received.

What is the product code of K895663?

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