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FDA 510(k)

VICTUS LASER PLATFORM

K-Number: K120426 · 2012-07-31

ApplicantTechnolas Perfect Vision GmbH
Decision Date2012-07-31
Product CodeOOE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VICTUS LASER PLATFORM is the device name listed in this FDA 510(k) record. The listed applicant is Technolas Perfect Vision GmbH. It received FDA 510(k) clearance on 2012-07-31 under 510(k) number K120426. The device is classified under product code OOE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICTUS LASER PLATFORM?

VICTUS LASER PLATFORM is a medical device that received FDA 510(k) clearance on 2012-07-31. The listed applicant is Technolas Perfect Vision GmbH. The 510(k) number is K120426.

When did VICTUS LASER PLATFORM receive FDA 510(k) clearance?

VICTUS LASER PLATFORM received FDA 510(k) clearance on 2012-07-31, under 510(k) number K120426.

Who is the listed applicant for VICTUS LASER PLATFORM?

The FDA 510(k) record lists Technolas Perfect Vision GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VICTUS LASER PLATFORM?

The FDA product code for VICTUS LASER PLATFORM is OOE.

Related Clinical Trials

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Other records listing Technolas Perfect Vision GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K200724VICTUS Femtosecond Laser PlatformK171014VICTUS Femtosecond Laser PlatformK122386VICTUS FEMTOSECOND LASER PLATFORMK110427FEMTEC LASER SYSTEM FOR CAPSULOTOMYK984443ORBSCAN

Related Devices (Code: OOE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252682LenSx Laser System (8065000944)Alcon Laboratories, Inc.K243896LenSx Laser System (8065998162)Alcon Laboratories, Inc.K223566ELITA™ Femtosecond Laser System, ELITA™ Patient InterfaceJohnson & Johnson Surgical Vision, Inc.K223838Catalys™ Precision Laser SystemAmo Manufacturing USA, LLCK220259ALLY Adaptive Cataract Treatment SystemLensar, Inc.K220516CATALYS Precision Laser systemAmo Manufacturing USA, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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