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FDA 510(k)

LFR-260

K-Number: K233295 · 2024-05-31

ApplicantEvolution Optiks Limited
Decision Date2024-05-31
Product CodeSBI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LFR-260 is a medical device manufactured by Evolution Optiks Limited. It received FDA 510(k) clearance on 2024-05-31 under approval number K233295. The device is classified under product code SBI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LFR-260?

LFR-260 is a medical device that received FDA 510(k) clearance on 2024-05-31. It is manufactured by Evolution Optiks Limited. The 510(k) number is K233295.

When was LFR-260 approved by the FDA?

LFR-260 received FDA 510(k) clearance on 2024-05-31, under approval number K233295.

What company makes LFR-260?

LFR-260 is manufactured by Evolution Optiks Limited.

What is the FDA product code for LFR-260?

The FDA product code for LFR-260 is SBI.

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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