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FDA 510(k)

VICTUS Femtosecond Laser Platform

K-Number: K200724 · 2020-09-01

ApplicantTechnolas Perfect Vision GmbH
Decision Date2020-09-01
Product CodeOOE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VICTUS Femtosecond 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 2020-09-01 under 510(k) number K200724. 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 Femtosecond Laser Platform?

VICTUS Femtosecond Laser Platform is a medical device that received FDA 510(k) clearance on 2020-09-01. The listed applicant is Technolas Perfect Vision GmbH. The 510(k) number is K200724.

When did VICTUS Femtosecond Laser Platform receive FDA 510(k) clearance?

VICTUS Femtosecond Laser Platform received FDA 510(k) clearance on 2020-09-01, under 510(k) number K200724.

Who is the listed applicant for VICTUS Femtosecond 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 Femtosecond Laser Platform?

The FDA product code for VICTUS Femtosecond Laser Platform is OOE.

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.

PMA P990027Excimer laser systemK171014VICTUS Femtosecond Laser Platform

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

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

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