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FDA 510(k)

VICTUS Femtosecond Laser Platform

K-Number: K171014 · 2017-10-19

ApplicantTechnolas Perfect Vision GmbH
Decision Date2017-10-19
Product CodeOOE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VICTUS Femtosecond Laser Platform is a medical device manufactured by Technolas Perfect Vision GmbH. It received FDA 510(k) clearance on 2017-10-19 under approval number K171014. 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 2017-10-19. It is manufactured by Technolas Perfect Vision GmbH. The 510(k) number is K171014.

When was VICTUS Femtosecond Laser Platform approved by the FDA?

VICTUS Femtosecond Laser Platform received FDA 510(k) clearance on 2017-10-19, under approval number K171014.

What company makes VICTUS Femtosecond Laser Platform?

VICTUS Femtosecond Laser Platform is manufactured by Technolas Perfect Vision GmbH.

What is the FDA product code for VICTUS Femtosecond Laser Platform?

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

Related Clinical Trials

NCT05231278 Confocal Laser Endomicroscopy Nodule Localization by Robotic Bronchoscopy COMPLETED NCT07036835 Clinical Investigation of a Femtosecond Laser for Corneal Flap Creation ACTIVE_NOT_RECRUITING NCT01638390 Use of the VisuMax™ Femtosecond Laser COMPLETED

Other Devices by Technolas Perfect Vision GmbH

K200724VICTUS Femtosecond Laser Platform PMA P990027Excimer laser system

Related Devices (Code: OOE)

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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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