Ophthalas 532 Solid State Photocoagulator, or Equivalent Laser Systems

FDA 510(k) K962592 · Alcon Laboratories

Substantially Equivalent

510(k) numberK962592

Submission

Device name
Ophthalas 532 Solid State Photocoagulator, or Equivalent Laser Systems
Applicant
Alcon Laboratories
Fort Worth, TX, US
Received
July 2, 1996
Decision date
September 23, 1996
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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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
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K261221SOLTIVE™ Laser System (SOLTIVE™ Pro SuperPulsed Laser, SOLTIVE™ Premium SuperPulsed…GEX · Traditional Olympus Surgical Technologies America07/24/2026SE
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Questions and answers

When was Ophthalas 532 Solid State Photocoagulator, or Equivalent Laser Systems cleared by the FDA?

Ophthalas 532 Solid State Photocoagulator, or Equivalent Laser Systems (K962592) received a 510(k) decision of Substantially Equivalent on September 23, 1996, 83 days after the submission was received.

What is the product code of K962592?

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