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FDA 510(k)

VISULAS green

K-Number: K232051 · 2023-10-24

ApplicantCarl Zeiss Meditec
Decision Date2023-10-24
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISULAS green is a medical device manufactured by Carl Zeiss Meditec. It received FDA 510(k) clearance on 2023-10-24 under approval number K232051. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISULAS green?

VISULAS green is a medical device that received FDA 510(k) clearance on 2023-10-24. It is manufactured by Carl Zeiss Meditec. The 510(k) number is K232051.

When was VISULAS green approved by the FDA?

VISULAS green received FDA 510(k) clearance on 2023-10-24, under approval number K232051.

What company makes VISULAS green?

VISULAS green is manufactured by Carl Zeiss Meditec.

What is the FDA product code for VISULAS green?

The FDA product code for VISULAS green is HQF.

Related Clinical Trials

NCT01638390 Use of the VisuMax™ Femtosecond Laser COMPLETED

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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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